Good Manufacturing Practice (GMP)

GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

What does GMP Covers?

GMP covers all aspects of the manufacturing process: defined manufacturing process; validated critical manufacturing steps; suitable premises, personal hygiene, 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.

How to Implement GMP?

Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process, every time a product is made.

Benefits of GMP:

Outlines the quality system that reduce and prevent errors
Ensures products are safe to use for humans
prevents/controls contamination or cross contamination
minimalizes variations in potency of the drug
prevents side effects and toxicity due to variations in drug contents and potency

What do we offer for GMP Certification for your organization?

With a team of highly qualified consultants and trainers having vast industrial experience, Vanguard Consulting & Inspection Services assists organizations across the world to implement and achieve GMO certification. Our consultation approach is highly professional, time bound and effective resulting in ease of implementation and adds value to the business processes of the client’s organization.

Contact us at info@vanguardconsultant.com to get your organization GMP certified.