GMP Certification in Uttam Nagar, Delhi

Good Manufacturing Practice (GMP) is a term that is recognized worldwide for the control and management of manufacturing, testing and overall quality control of food and pharmaceutical products. GMP takes quality assurance approach, which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization. GMP is aimed primarily at diminishing the risks inherent in any Pharmaceutical or Food production.Benefits of GMP : It is believed that GMP is a good business tool, which will help to refine both compliance and performance of the Company. GMP requirements are largely common sense practices, which will help companies better itself as it moves toward a quality approach using continuous improvement. GMP is also sometimes referred to as “cGMP”. The “current,” methodologies of manufacture, testing, design and control. The Manufacturers must employ technologies and systems, which are up-to-date. Systems and equipment used to prevent contamination, mixups, and errors are adequate by today’s standards. Thus, Good Manufacturing Practices GMP, when certified of an organization, is an authorization and certification of Companies product & process that quality standards are adequate, up to date and controlled for the intended use by the consumer. How can DBS CERT help? DBS CERT consists of full-time trainers and certification with a unique combination of manufacturing experience, business and financial expertise, A “hands-on” approach creates a recipe for our clients’ success. System Study, Documentation-GMP Manual Preparation, Records Implementation, GMP Trainings, Internal Audits.  Clients choose us! : Bring world-class quality standards to your business : Specialized in ISO certification,ISO Documentatiom,ISO Record, Iso Implementation, ISO Internal Auditing, ISO Certification, CE Marking, Training-Internal Auditing / is based in Mumbai,delhi, nce, India, Singapore, Tanzania, Nigeria, UK, Saudi Arabia, Sri Lanka, UAE

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GMP Certification, iso 9001 2008 certification Consultant

W.h.o. Defines good manufacturing practices (gmp) as "that part of quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization". Gmp covers all aspects of the manufacturing process: defined manufacturing process; validated critical manufacturing steps; suitable premises, storage, transport; qualified and trained production and quality control personnel; adequate laboratory facilities; approved written procedures and instructions; records to show all steps of defined procedures taken; full traceability of a product through batch processing records and distribution records; and systems for recall and investigation of complaints. the guiding principle of gmp is that quality is built into a product, and not just tested into a finished product. Therefore, the assurance is that the product not only meets the final specifications, but that it has been made by the same procedures under the same conditions each and every time it is made. There are many ways this is controlled - controlling the quality of the facility and its systems, controlling the quality of the starting materials, controlling the quality of production at all stages, controlling the quality of the testing of the product, controlling the identity of materials by adequate labeling and segregation, controlling the quality of materials and product by adequate storage, etc. All of these controls must follow prescribed, formal, approved procedures, written as protocols, sops, or master formulae, describing all the tasks carried out in an entire manufacturing and control process. gmp covers all aspects of the manufacturing process including : • defined manufacturing process • validated critical manufacturing steps • suitable premises, storage, transport, qualified and trained production and quality control personnel • adequate laboratory facilities • approved written procedures and instructions • records to show all steps of defined procedures have been taken • full traceability of a product through batch records and distribution records • systems for recall and investigation of complaints.

The guiding principle of gmp is that quality is built into a product, and not just tested into a finished product. Therefore, the assurance is that the product not only meets the final specifications, but that it has been made by the same procedures under the same conditions each and every time it is made. There are many ways this is controlled - controlling the quality of the facility and its systems, controlling the quality of the starting materials, controlling the quality of production at all stages, controlling the quality of the testing of the product, controlling the identity of materials by adequate labeling and segregation, controlling the quality of materials and product by adequate storage, etc. All of these controls must follow prescribed, formal, approved procedures, written as protocols, sops, or master formulae, describing all the tasks carried out in an entire manufacturing and control process. gmp covers all aspects of the manufacturing process including : • defined manufacturing process • validated critical manufacturing steps • suitable premises, storage, transport, qualified and trained production and quality control personnel • adequate laboratory facilities • approved written procedures and instructions • records to show all steps of defined procedures have been taken • full traceability of a product through batch records and distribution records • systems for recall and investigation of complaints