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Welcome to Crescent Quality Certification
More Then 25 Years Experience
Crescent Quality Certification is a bonafide and reliable place where you can get all the services for your company like ISO Certification, products/ compliance certificate and training etc. We provide you all these services at the cheapest and inexpensive prices. Our charges are low-cost and affordable that any entrepreneur can afford our services.
We also provide help and guidance regarding conditions and procedures for establishing new startups for aspiring entrepreneurs or those who wish to build their own company. We promise to give you quicker results.
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Our Top Services
ISO CERTIFICATION
+To cater demands of clients, we are highly engrossed in offering ISO Certification Our highly skilled lead auditor/ professionals check this certification service on quality parameters before offering to clients. In addition to this, an offered array of training services is rendered using the latest technology.
COMPLIAMCE CERTIFICATION
+Backed with years of experience in this domain, we have been able to offer a large collection of products and compliance Certificate Service. These certificate services are rendered using top-grade resources. Offered certificate services are admired due to their reasonable price, and client-focused approach.
TRAINING
+Training in allied areas like Lead Auditor, Internal Auditor & awareness courses, 5S & tailor made courses. CQC also deals in Third Party Inspection, Product Certification (CE), Automotive Homologation, Six Sigma and compliance certification for HALAL, GMP, KOSHER, ORGANIC, GOTS, CMMI LEVEL, HACCP etc.
ISO
Quality Certification
ISO stands for International organization for standardization which certifies that a management system of a Manufacturing process or service and its documentation procedures contains all the requirements for standardization and quality assurance. ISO is an independent and international organization that establishes standards to ensure the safety, quality, and efficiency of products, and services. ISO was established on February 23rd, 1947. The ISO is headquarters in Geneva, Switzerland. ISO publishes the different types of standards to improve the quality and safety of products and services.ISO 9001:2015, ISO 14001:2015, OHSAS 18001:2007, ISO 45001:2018, ISO 20000- 1:2011, ISO 27001:2013, ISO 22000:2005, ISO 22000:2018, ISO 50001:2011 and ISO 13485:2016 and FSSC 22000, ISO 39001:2012, ISO 21898:2004, ISO/IEC 27018:2014, ISO 10668:2010, ISO 21001:2018, ISO 10004:2018, ISO 10002:2018, ISO 20121:2012, ISO 22301:2012, Iso 37001:2016, ISO 55001:2014, ISO 29990:2010, ISO 41001:2018, ISO 20000-1:2018.
The ISO 9001 standard requirements are generic and are intended to be applicable to any type of organization, regardless of its type or size, or the products and services it provides. World first ISO standards which is most acceptable in market globally.
ISO 9001:2015 Quality Management System (QMS) is internationally recognized as the world’s leading quality management standard and has been implemented by over one million organizations in over 170 countries globally. ISO 9001 implemented, to its full potential, becomes an invaluable asset to your organization.
The purpose of the standard is to assist companies in meeting statutory and regulatory requirements relating to their product while achieving excellence in their customer service and delivery. The standard can be used throughout an organization to improve the performance or within a particular site, plant or department.
ISO 9001 contains eight key principles of quality management which is not auditable but do form the fundamental characteristics of quality management.
ISO 14001 Environmental Management System (EMS) is a systematic framework to manage the immediate and long term environmental impacts of an organization’s products, services and processes. By completing ISO 14001 certification your organization can assure stakeholders that your environmental management system meets international industry specific environmental standards.
Environmental regulations are getting stricter, and so is the law enforcement. Customers and shareholders increasingly demand that businesses diminish the environmental impact from their business, demonstrate what they do, and how they improve.
An Environmental Management System helps your organization to be in control of and successfully manage the most significant environmental aspects, e.g. emissions, waste-handling, utilize natural resources, and energy-efficiency.
ISO 45001:2018 Occupational Health and Safety Management Certification is an international standard which provides a framework to identify, control and decrease the risks associated with health and safety within the workplace. Implementing the standard will send a clear signal to your stakeholders that you view employee’s health and safety as a priority within your organization.
An increasing number of organizations are completing ISO 45001 certification as employers are under increasing pressure to ensure that a rigorous health and safety policy is in place which protects employees against possible occupational risks and reduces the likelihood of accidents in the workplace.
By planning ahead an organization can also identify health and safety risks and conform to health and safety legislation.
International Organization for Standardization (ISO) published the new standard – Food Safety Management Systems – Requirements for any organization in the food chain. There has been a continuous increase in consumer demand for safe food. This has led to the development of various foods safety standards. The growing number of national standards has led to confusion. Consequently, there is a need for international harmonization and ISO aims to meet this need with ISO 22000:-
The standard is complimentary to ISO9001, in that ISO 22000 addresses specifically the issues relating to food safety and uses an approach that can be integrated with that of ISO 9001. ISO 22000 is not a replacement for ISO 9001, however businesses in the food sector may see it as having greater commercial importance to their business than ISO 9001, particularly as there is increasing pressure on the food industry to demonstrate that it is effectively managing food safety, following the highly publicized food scares around the world.
ISO 22000:2018stands for food safety management system. It is a prevention-based food safety system that identifies and prevents microbial, chemical and other hazards in the food based industry.
ISO 27001 is the international standard which is recognized globally for managing risks to the security of information you hold. Certification to ISO 27001 allows you to prove to your clients and other stakeholders that you are managing the security of your information. ISO 27001:2013 (the current version of ISO 27001) provides a set of standardized requirements for an Information Security Management System (ISMS). The standard adopts a process based approach for establishing, implementing, operating, monitoring, maintaining, and improving your ISMS.
ISO/IEC 27001, part of the growing ISO/IEC 27000 family of standards, is an Information Security Management System (ISMS) standard published in October 2013 by the International Organization for Standardization (ISO) and the International Electro technical Commission (IEC). Its full name is ISO/IEC 27001:2013 – Information technology — Security techniques — Information security management systems — Requirements but it is commonly known as “ISO 27001”.
ISO/IEC 27001 formally specifies a management system that is intended to bring information security under explicit management control.
ISO 21001:2018 specifies requirements for a management system for educational organizations (EOMS) when such an organization: 1.Needs to demonstrate its ability to support the acquisition and development of competence through teaching, learning or research 2.Aims to enhance satisfaction of learners, other beneficiaries and staff through the effective application of its EOMS, including processes for improvement of the system and assurance of conformity to the requirements of learners and other beneficiaries.
All requirements of ISO 21001:2018 are generic and intended to be applicable to any organization that uses a curriculum to support the development of competence through teaching, learning or research, regardless of the type, size or method of delivery.
ISO 21001:2018 can be applied to educational organizations within larger organizations whose core business is not education, such as professional training departments. ISO 21001:2018 does not apply to organizations that only produce or manufacture educational products.
ISO/IEC 20000 is an Information Technology Service Management (ITSM) the first World Wide International standard for IT service management. It was developed in 2005, by ISO/IEC JTC1 SC7 and revised in 2011. It is based on and intended to supersede the earlier BS 15000 that was developed by BSI Group.
Formally: ISO/IEC 20000-1:2018 (‘part 1’) includes the design, transition, delivery and improvement of services that fulfill service requirements and provide value for both the customer and the service provider. This standard requires an integrated process approach when the service provider plans, establishes, implements, operates, monitors, review, maintains and improves a Service Management System (SMS). This is an international IT standard that allows companies to demonstrate excellence and prove best practice in IT management. The standard ensures companies can achieve evidence-based benchmarks to continuously improve their delivery of IT services. The adoption of this standard has grown quite rapidly in the international arena of IT service providers and it has become a competitive differentiator for delivery of IT services. It is aligned with and complementary to the process approach defined within ITIL from the Office of Government Commerce (OGC).
Facilities management (FM) is understood to suffer from a general lack of knowledge and awareness, thus the publication of these supporting documents to articulate “what it is” was seen to be extremely beneficial. ISO 41011:2017 describes facility management as an "organizational function which integrates people, place and process within the built environment with the purpose of improving the quality of life of people and the productivity of the core business".
Benefits of ISO 41001:2018
improved safety, health, well-being and productivity of workforce. better efficiency and effectiveness, hence improving organisational cost benefits. enhanced communication of FM methodologies and requirements among and between public and private sector organizations. improved consistency of service levels delivered.
FSSC 22000 is a Food Safety Management System (FSMS) Certification Scheme. The FSSC 22000 System was designed to provide companies in the food industry with an ISO-based food safety management system certification that is recognized by the Global Food Safety Initiative (GFSI). Recognition by GFSI provides worldwide recognition and acceptance by food manufacturers and retailers. FSSC 22000 defines requirements for integrated processes that work together to control and minimize food safety hazards.
Benefits of FSSC 22000
FSSC 22000 Is an ISO based Food Safety Management System and it integrates nicely with other ISO based management systems including ISO 9001, ISO 14000 and others.
Managing Risk
First and foremost, building an FSSC System will provide your company with effective management of food safety hazards by creating an environment capable of producing safe product and a management system to continually manage, monitor, validate and improve the system.
PQC has implemented SA-8000 Certification in more than 100+ organization across the India. We have a team of auditors who are expertise in Implementation, Training & Auditing.
What is SA-8000:2014?
SA stands for Social Accountability, 8000 is the standard & 2014 is the revision of year. This is a social compliance certification standard that encourages organizations to develop, maintain and apply socially acceptable practices in the workplace & provide common guidelines for worker in hiring, remuneration, access to training, promotion, termination or retirement not based on race, national or territorial or social origin, caste, birth, religion, disability, gender, sexual orientation, family responsibilities, marital status, union membership, political opinions, age or any other condition that could give rise to discrimination.
IATF 16949:2016 is an internationally recognized Quality Management System specification for the automotive industry. IATF 16949: 2016 is the current version of the standard that was developed for the Automotive Industry. It contains all of the requirements of ISO 9001 plus several additional requirements specifically for the Automotive Industry.
Benefits of IATF 16949:2016
Internal
implementation and enhancement of documentation .
systematization of management activities and processes .
full customer-orientation .
enhancement of processes .
improvement of products quality .
reduction of the amount of shortages and repairs .
increase of effectiveness and productivity
ISO 39001:2012 specifies requirements for a road traffic safety (RTS) management system to enable an organization that interacts with the road traffic system to reduce death and serious injuries related to road traffic crashes which it can influence. The requirements in ISO 39001:2012 include development and implementation of an appropriate RTS policy, development of RTS objectives and action plans, which take into account legal and other requirements to which the organization subscribes, and information about elements and criteria related to RTS that the organization identifies as those which it can control and those which it can influence.
What is ISO 39001?
As an international standard, ISO 39001 specifies the requirements for Road Traffic Safety Management Systems. Additionally, it serves as a tool for organizations to reduce and eventually eliminate accidents, deaths and severe injuries associated with road traffic crashes. Road Traffic Safety (RTS) is considered as a global issue, as the number of accidents that occur worldwide is constantly rising. Therefore, firms and/or individuals, who are committed to improving road safety and offer quality, will benefit from the implementation of ISO 39001. This standard identifies improved elements of road traffic safety, which enable organizations to reach their desired outcomes.
ISO 13485 is a stand-alone QMS standard, derived from the internationally recognized and accepted ISO 9000 quality management standard series. ISO 13485 adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. While ISO 13485 is based on the ISO 9001 process model concepts of Plan, Do, Check, Act, it is designed for regulatory compliance. Thus it is more prescriptive in nature and requires a more thoroughly documented quality management system.
ISO 13485 was written to support medical device manufacturers in designing quality management systems that establish and maintain the effectiveness of their processes. It ensures the consistent design, development, production, installation, and delivery of medical devices that are safe for their intended purpose. A medical device organization can implement to help demonstrate compliance to laws and regulations of the medical device industry.
ISO 13485 was written to support medical device manufacturers in designing quality management systems that establish and maintain the effectiveness of their processes. It ensures the consistent design, development, production, installation, and delivery of medical devices that are safe for their intended purpose.
Learning Services outside Formal Education- Service Requirements for LSP (Learning Service Provider)
What is ISO 29990:2010 Certification This standard specifies requirements for learning services outside formal education, including all types of life-long learning (e.g. vocational training and in-company training, either outsourced or in-house). These include any learning services provided by a learning service provider (LSP) that are addressed to learners themselves, as well as to sponsors who are acquiring the services on behalf of the learners. The key features of these kinds of services are that the goals of learning are defined and the services are evaluated, and that they involve interaction with the learner. The learning can be face-to-face, mediated by technology, or a blend of both.
In cases where the learning service provider is part of an organization that delivers products (i.e. goods and services) in addition to learning services, This standard only applies to learning services. This standard is not aimed at schools, colleges and universities providing learning services as part of a formal education system, but it can be useful to them as a tool for reflection and self-evaluation.
ISO 55001:2014 is the new international standard designed to help organizations implement an anti-bribery management system. It specifies a series of measures your organization can implement to help prevent, detect and address bribery.
In the age of transparency, no organization can afford to take the risk of bribery lightly. Investors, business associates, personnel and shareholders all need to be assured that the management has made every possible effort to prevent bribery at all levels of the organization. Implementing the ISO 37001 and certification through an independent third party enables you to do exactly that.
The ISO 55001:2014 standard is designed to help an organization implement and maintain a proactive anti-bribery system. The standard, which replaced the British Standard 10500, provides a number of requirements that represent globally recognized good practice for anti-bribery. The standard is applicable to all kinds of organizations.
The 2018 version of ISO 50001 was released on 21 August 2018. With this release, ISO 50001:2011 will be withdrawn. The transition deadline is confirmed by the International Accreditation Forum (IAF) to be three years from the publication date. To keep a certificate valid after this deadline, companies need to make sure their certificate is transitioned during the 3-year period.
It is also proposed to be in line with ISO 9001 and ISO 14001 standards that address quality management and environmental management issues. Also, it will have the common elements of ISO’s management standards like the continual improvement vide Plan-Do-Check-Act method adopted in the earlier ISO Management standards.
Its implementation is expected to address what the organization does to effectively manage energy resources and performance that is relevant to global standards.
ISO 20121:2012 specifies requirements for an event sustainability management system for any type of event or event-related activity, and provides guidance on conforming to those requirements.
ISO 20121:2012 is applicable to any organization that wishes to:
establish, implement, maintain and improve an event sustainability management system;
ensure that it is in conformity with its stated sustainable development policy;
Demonstrate voluntary conformity with ISO 20121:2012 by
first party (self-determination and self-declaration),
second party (confirmation of conformance by parties having an interest in the organization, such as clients, or by other persons on their behalf), or independent third party (e.g. a certification body).
ISO 20121:2012 has been designed to address the management of improved sustainability throughout the entire event management cycle .
ISO 37001 is the new international standard designed to help organizations implement an anti-bribery management system. It specifies a series of measures your organization can implement to help prevent, detect and address bribery.
In the age of transparency, no organization can afford to take the risk of bribery lightly. Investors, business associates, personnel and shareholders all need to be assured that the management has made every possible effort to prevent bribery at all levels of the organization. Implementing the ISO 37001 and certification through an independent third party enables you to do exactly that.
The ISO 37001 standard is designed to help an organization implement and maintain a proactive anti-bribery system. The standard, which replaced the British Standard 10500, provides a number of requirements that represent globally recognized good practice for anti-bribery. The standard is applicable to all kinds of organizations.
ISO/IEC 27018:2014 establishes commonly accepted control objectives, controls and guidelines for implementing measures to protect Personally Identifiable Information (PII) in accordance with the privacy principles in ISO/IEC 29100 for the public cloud computing environment. In particular, ISO/IEC 27018:2014 specifies guidelines based on ISO/IEC 27002, taking into consideration the regulatory requirements for the protection of PII which might be applicable within the context of the information security risk environment(s) of a provider of public cloud services.
ISO/IEC 27018:2014 is applicable to all types and sizes of organizations, including public and private companies, government entities, and not-for-profit organizations, which provide information processing services as PII processors via cloud computing under contract to other organizations.
The guidelines in ISO/IEC 27018:2014 might also be relevant to organizations acting as PII controllers; however, PII controllers can be subject to additional PII protection legislation, regulations and obligations, not applying to PII processors. ISO/IEC 27018:2014 is not intended to cover such additional obligations.
ISO 22301 is the international standard for business continuity management, and was built on the success of British Standard BS 25999 and other regional standards. It’s designed to protect your business from potential disruption. This includes extreme weather, fire, flood, natural disaster, theft, IT outage, staff illness or terrorist attack. The ISO 22301 management system lets you identify threats relevant to your business and the critical business functions they could impact. It allows you to put plans in place ahead of time to ensure your business doesn’t come to a standstill. Business Continuity Management must be a board level responsibility and business continuity planning needs to be business-led. These statements are supported by BS 25999, the Business Continuity Management Standard, which was launched in 2006.
Benefits of 22301:2012
Business Continuity Management helps you identify the threats to your business. This means you can take a proactive approach to minimize the impact on your business when a disaster occurs . With an ISO 22301 business continuity management system framework, you can ensure the continuity of critical functions which can be the difference between a business surviving or failing. With ISO 22301 you can become a more resilient organization, whatever your business.
ISO 21898:2004 specifies materials, construction and design requirements, type test, certification and marking requirements for flexible intermediate bulk containers (FIBCs) intended to contain non-dangerous solid materials in powder, granular or paste form, and designed to be lifted from above by integral or detachable devices.
ISO 10668:2010 specifies requirements for procedures and methods of monetary brand value measurement.
ISO 10668:2010 specifies a framework for brand valuation, including objectives, bases of valuation, approaches to valuation, methods of valuation and sourcing of quality data and assumptions.
It also specifies methods for reporting the results of such valuation.
ISO 10004:2018 This document gives guidelines for the process of complaints handling related to products and services within an organization, including planning, design, development, operation, maintenance and improvement. The complaints-handling process described is suitable for use as one of the processes of an overall quality management system.
NOTE Throughout this document, the terms “product” and “service” refer to the outputs of an organization that are intended for, or required by, a customer.
This document is intended for use by any organization regardless of its type or size, or the products and services it provides. It is also intended for use by organizations in all sectors. Annex B provides guidance specifically for small businesses.
ISO 10002:2018 This document gives guidelines for the process of complaints handling related to products and services within an organization, including planning, design, development, operation, maintenance and improvement. The complaints-handling process described is suitable for use as one of the processes of an overall quality management system.
NOTE Throughout this document, the terms “product” and “service” refer to the outputs of an organization that are intended for, or required by, a customer.
This document is intended for use by any organization regardless of its type or size, or the products and services it provides. It is also intended for use by organizations in all sectors. Annex B provides guidance specifically for small businesses.
Compliance
Certification
Backed with years of experience in this domain, we have been able to offer a large collection of products and compliance Certificate Service. These certificate services are rendered using top-grade resources. Offered certificate services are admired due to their reasonable price, and client-focused approach.BIFMA’s level is the multi-attribute sustainability standard and third-party certification program for the commercial furniture industry. BIFMA developed level to deliver an open and holistic means of evaluating and communicating the environmental and social impacts of furniture products in the built environment. Taking into account a company’s social actions, energy usage, material selection, human and ecosystem health, along with numerous other impacts, level addresses how a product is sustainable from multiple perspectives.
About BIFMA
BIFMA is the not-for-profit trade association for business and institutional furniture manufacturers. Since 1973, BIFMA’s role has been to sponsor the development and refining of current and future standards, educate on their importance and application, and translate their necessary complexity into more easily understood and implemented formats. We also monitor the state of the industry, serve as a forum for member cooperation and collaboration, interact with international counterparts, and advocate for regulatory conditions that foster value and innovation.
What is CE Marking (CE Mark)?
CE Marking is the symbol as shown on the top of this page. The letters “CE” are the abbreviation of French phrase “Conformité Européene” which literally means “European Conformity”. The term initially used was “EC Mark” and it was officially replaced by “CE Marking” in the Directive 93/68/EEC in 1993. “CE Marking” is now used in all EU official documents.
“CE Mark” is also in use, but it is NOT the official term. For instance, in the Directive 2007/47/ec, of 5 September 2007, amending the directives 90/385/eec, 93/42/eec & 98/8/ec, the term CE Marking appears 9 times whereas CE Mark appears nowhere in the entire 35-page document. CE Marking on a product is a manufacturer’s declaration that the product complies with the essential requirements of the relevant European health, safety and environmental protection legislation, in practice by many of the so-called Product Directives. *Product Directives contains the “essential requirements” and/or “performance levels” and “Harmonized Standards” to which the products must conform. Harmonized Standards are the technical specifications (European Standards or Harmonization Documents) which are established by several European standards agencies (CEN, CENELEC, etc).
At maturity level 3, an organization has achieved all the specific and generic goals of the process areas assigned to maturity
levels 2 and 3
At maturity level 3, processes are well characterized and understood, and are described in standards, procedures, tools, and methods.
A critical distinction between maturity level 2 and maturity level 3 is the scope of standards, process descriptions, and procedures. At maturity level 2, the standards, process descriptions, and procedures may be quite different in each specific instance of the process (for example, on a particular project). At maturity level 3, the standards, process descriptions, and procedures for a project are tailored from the organization’s set of standard processes to suit a particular project or organizational unit. Another critical distinction is that at maturity level 3, processes are typically described in more detail and more rigorously than at maturity level 2. At maturity level 3, processes are managed more proactively using an understanding of the interrelationships of the process activities and detailed measures of the process, its work products, and its services.
At maturity level 4, an organization has achieved all the specific goals of the process areas assigned to maturity levels 2, 3, and 4 and the generic goals assigned to maturity levels 2 and 3. At maturity level 4 Subproce
sses are selected that significantly contribute to overall process performance. These selected subprocesses are controlled using statistical and other quantitative techniques. Quantitative objectives for quality and process performance are established and used as criteria in managing processes. Quantitative objectives are based on the needs of the customer, end users, organization, and process implementers. Quality and process performance are understood in statistical terms and are managed throughout the life of the processes.
For these processes, detailed measures of process performance are collected and statistically analyzed. Special causes of process variation are identified and, where appropriate, the sources of special causes are corrected to prevent future occurrences. Quality and process performance measures are incorporated into the organization.s measurement repository to support fact-based decision making in the future. A critical distinction between maturity level 3 and maturity level 4 is the predictability of process performance. At maturity level 4, the performance of processes is controlled using statistical and other quantitative techniques, and is quantitatively predictable. At maturity level 3, processes are only qualitatively predictable.
At maturity level 5, an organization has achieved all the specific goals of the process areas assigned to maturity levels 2, 3, 4, and 5 and the generic goals assigned to maturity levels 2 and 3.
Processes are continually improved based on a quantitative understanding of the common causes of variation inherent in processes.
Maturity level 5 focuses on continually improving process performance through both incremental and innovative technological improvements.
Quantitative process-improvement objectives for the organization are established, continually revised to reflect changing business objectives, and used as criteria in managing process improvement. The effects of deployed process improvements are measured and evaluated against the quantitative process-improvement objectives. Both the defined processes and the organization’s set of standard processes are targets of measurable improvement activities.
Optimizing processes that are agile and innovative depends on the participation of an empowered workforce aligned with the business values and objectives of the organization. The organization’s ability to rapidly respond to changes and opportunities is enhanced by finding ways to accelerate and share learning. Improvement of the processes is inherently part of everybody’s role, resulting in a cycle of continual improvement.
Good manufacturing practice (GMP) is a concept that ensures products are consistently produced and controlled according to quality standards. It is designed to minimize the risks to the patient involved in any pharmaceutical production.
GMP constitutes the license to operate in pharmaceutical manufacturing, and is a core condition worldwide. However, rules and interpretations differ from country to country and change frequently. Therefore, having fully trained experts at hand to help with the implementation of these rules is very important.
Benefits of GMP
Costs reduced and resources saved.
Evidence of safe and efficient food handling.
Compliance with legal requirements and builds customer trust.
India Organic Certification is a label given to organic products after validation, which ensures that the product or raw materials used in the product were grown through organic farming – without any chemical fertilizers, pesticides, or induced hormones. A trademark – "India Organic" will be granted on the basis of compliance with the National Standards for Organic Production.
Communicating the genuineness as well as the origin of the product, this trademark will be owned by the Government of India. The National Standards for Organic Products was established in 2000 which ensures the authenticity of the organic product. PQC is providing the compliance certifications for the organic standard.
Organic Farming Requirements Any farm which proposes to obtain the Organic Farm certification must conform to the following standards set out by the National Programme for Organic Production (NPOP).
The Global Organic Textile Standard (GOTS) is the worldwide leading textile processing standard for organic fibres, including ecological and social criteria, backed up by independent certification of the entire textile supply chain.
Version 5.0 was published on 1st of March 2017, 3 years after the Version 4.0 was introduced and 12 years after the launch of the 1st Version. The high ecological and social requirements as well as worldwide practicability and verifiability were considered in the revision work, in order to achieve a reliable and transparent set of criteria.
The information in this section provides an overview of the content and basic requirements of the standard. It does not reflect all criteria of the standard and can therefore not be used for any official purpose.
Hazard Analysis and Critical Control Points(HACCP) is a management system used in the food industry and this chapter describes basic HACCP principles along with a few details from the more recent Hazard Analysis and Risk-Based Preventive Controls system variation.
The US Food and Drug administration created four food-specific websites describing important details for diary, juice, retail/food service, and seafood HACCP programs.
These programs and efforts to teach how to control food risks will be discussed, including alleged violations of HACCP regulations, which are illustrated in food-related Warning Letters and publications citing needs for improved HACCP execution. Topics include information on hazards associated with juice and seafood, pest control, and drug residues in dairy products.
Halal is a term from Quran that means “permitted” or "lawful". Therefore, in relation to food, Halal is used for food and other consumables that are permissible for consumption and used by Muslims, based on the Islamic law, the Shariah.
Halal promotes cleanliness in all aspects of a person and halal foods ensure that food consumed by a person in their daily lives are clean, hygienic and not detrimental to their health or well-being. Having a halal certification ensures that the food product is deemed safe for consumption and with rising awareness about Halal foods, more and more businesses are seeking Halal Certification for their products, premises, restaurants, etc., In this article, we look at the procedure for obtaining Halal Certification in India.
Halal Certification Halal India Private Limited
Halal Certification Services India Private Limited
Jamiat Ulama-E-Maharashtra – a State unit of Jamiat Ulama-E-Hind
Jamiat Ulama-i-Hind Halal Trust
PQ Certifications is India’s premier kosher certification agency having office in Delhi. We have affiliations with different kosher certification agencies / rabbi’s to provide kosher food certification services across India and globe in their supervision in best possible manner at affordable rates. This makes us leader in kosher food certification in India with combined experience of certifying more than 50,000 products and more than 1000 production facilities across the world. Think Kosher Think PQC has become synonymous.
Our objective is to help small and medium enterprise to go for kosher certificate.
What is Kosher?
Kosher is another term for kashrut, or Jewish dietary law.
Kosher foods are prepared following strict kashrut guidelines, which can vary in different Jewish communities, but have the same basic rules. Jewish dietary laws were established in the Old Testament of the Bible, with additional rabbinical decrees handed down through generations.
REACH is a regulation of the European Union, adopted to improve the protection of human health and the environment from the risks that can be posed by chemicals, while enhancing the competitiveness of the EU chemicals industry. It also promotes alternative methods for the hazard assessment of substances in order to reduce the number of tests on animals.
If you are a manufacturer or formulator of chemical substances or import them from outside the European Union, you may have registration obligations under the REACH regulation. REACH stands for the regulation concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (EC) No 1907/2006 (REACH). It came into force on 1st June 2007 and replaced a number of European directives and regulations with a single system.
REACH applies to all chemical substances, not only those used in chemical processes but also for end-consumer use – even if not hazardous -, for example in paints, as well as in articles such as clothes and furniture. Therefore, the regulation has a wide impact on the compliacne of most companies that deal with products for the EU-market.
What is RoHS? RoHS stands for Restriction of Hazardous Substances. RoHS, also known as Directive 2002/95/EC, originated in the European Union and restricts the use of specific hazardous materials found in electrical and electronic products (known as EEE). All applicable products in the EU market after July 1, 2006 must pass RoHS compliance.
What are the restricted materials mandated under RoHS?
The substances banned under RoHS are lead (Pb), mercury (Hg), cadmium (Cd), hexavalent chromium (CrVI), polybrominated biphenyls (PBB), polybrominated diphenyl ethers (PBDE), and four different phthalates (DEHP, BBP, BBP, DIBP).
Why is RoHS compliance important?
The restricted materials are hazardous to the environment and pollute landfills, and are dangerous in terms of occupational exposure during manufacturing and recycling.
The ISO 9001 standard requirements are generic and are intended to be applicable to any type of organization, regardless of its type or size, or the products and services it provides. World first ISO standards which is most acceptable in market globally.
ISO 9001:2015 Quality Management System (QMS) is internationally recognized as the world’s leading quality management standard and has been implemented by over one million organizations in over 170 countries globally. ISO 9001 implemented, to its full potential, becomes an invaluable asset to your organization.
The purpose of the standard is to assist companies in meeting statutory and regulatory requirements relating to their product while achieving excellence in their customer service and delivery. The standard can be used throughout an organization to improve the performance or within a particular site, plant or department. ISO 9001 contains eight key principles of quality management which is not auditable but do form the fundamental characteristics of quality management.
ISO 16603:2004 describes a laboratory test method for measuring the penetration resistance of clothing materials to blood and body fluids. This test method uses a synthetic blood in continuous contact with the material specimen at specified set of conditions using the ISO 13994 test apparatus.
This test method is not always effective in testing protective clothing materials having thick, inner liners which readily absorb the synthetic blood.
ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees.
Each member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
Training
Training
Training in allied areas like Lead Auditor, Internal Auditor & awareness courses, 5S & tailor made courses. CQC also deals in Third Party Inspection, Product Certification (CE), Automotive Homologation, Six Sigma and compliance certification for HALAL, GMP, KOSHER, ORGANIC, GOTS, CMMI LEVEL, HACCP etc.P Q Certifications offers ISO lead auditor training courses in association with Empowering Assurance System in India . We conduct our QMS lead auditor training, ISO Training programs in Chennai, Bangalore, Mumbai, Hyderabad, Coimbatore, Pune, Ahmedabad, Kolkata, New Delhi, Kochi and other cities.
Enrolling yourself in the ISO Lead Auditor Training will help you get certified as an auditor for conducting audits. The course will get you focused on bringing in quality standards in business processes which will aid in both the development of self and the organization. Our lead auditor training is conducted as a 40 hour course that’s spread across five days. The QMS lead auditor Training delivered by the highly skilled and experienced authorities who practically engage in the assessment, audit and issuance of ISO certification on daily basis. With this, you will get the right and latest information about the procedures and policies followed.
ISO Lead Auditor :- ISO 9001:2015 QMS, ISO 27001:2013 ISMS, ISO 22000:2005 FSMS
P Q Certifications provides Internal auditor training Courses customised to suit your needs. All International Management Standards require to conduct internal auditors training as per ISO 19011 standard requirements. We prepare Case studies and examples based on the data collected from your company. Our training programmes are designed to bring out the best in you. Course material is provided in advance so that you can come prepared for the training. Our Power Point Presentations are easy, to understand and are very interactive. Our training would include workshops, role play, and an examinations at the end of the training.
ISO Internal Auditor Training – Objectives
The purpose of this program is to provide training in the principles, concepts and requirements of the standards.
On Completion of the course the participants will be able to :
Understand the underlying philosophy and use principles, concepts and requirements of the ISO standards and how to apply them within and auditing context. Carry out internal audits, with confidence and as per the requirement of ISO 19011.
Course Objectives The purpose of this program is to create awareness about the standards and the need for them in the Organization. The participants shall understand the prospects of a company that has achieved these standards.
Course Highlights
» ISO history and development.
» Purpose of policy and manuals needed.
» Why ISO?
» Where to start?
» Steps for certification An overview.
» Introduction about the certifying bodies and getting assistance.
Benefits
On completion of this course the participant shall be able to understand the importance of getting ISO certification, for the company and the benefits gained by the Organization thanks to it.
About the course
ISO is an ISO approved standard that enables an organization to implement and certify Information Security Management System (ISMS). The objective of this course is to prepare you in becoming an ISO Implementer.
Who should attend this training?
The course has been designed for those wishing to: To understand the fundamental concept of ISMS auditing
Become Internal ISMS Implementer
Extend and develop their previous knowledge of quality, systems and auditing skills
These programs and efforts to teach how to control food risks will be discussed, including alleged violations of HACCP regulations, which are illustrated in food-related Warning Letters and publications citing needs for improved HACCP execution. Topics include information on hazards associated with juice and seafood, pest control, and drug residues in dairy products.
Technical Training Course brings the knowledge to your location, resulting in immediate benefits for your team. This option is convenient for scheduling and provides an opportunity to train the whole team how to develop and implement the QMS. Onsite training is most popular with organizations that require five or more participants to be trained. Expenses are minimal compared to having the team travel. The training is conducted in a dynamic instructor-led format. The Quality-One reference materials and examples also provide an invaluable resource for review long after the training.
Executive Overview
This course provides a basic level of understanding of the ISO 9001 intent and requirements, as well as how the requirements can be met. Each participant will have the opportunity to be involved in exercises such as: SWOT Analysis, Seven Quality Management Principles, Defining the Organizations Context, Defining Interested Parties and their requirements, Systems Mapping (process approach). All activities will include industry-specific examples and terminology.
