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Good Manufacturing

Practice (GMP)

Good Manufacturing Practice (GMP)

Describes a set of principles and procedures that when followed helps ensure that therapeutic goods are of high quality.
  • We can also help you to perform the Analytical Studies, Validation, & Spectral Studies for Active Ingredients (APIs) and Formulations. Our Panel of Experts is having rich experience in setting up systems like GMP as per WHO / USFDA / MHRA / MCC/PMDA/MHLW / ICH guidelines as well GCP / GLP compliance as per ICH Guidelines.
  • We also undertake total turnkey basis project for GMP Compliance, starting from Plant Design to GMP Approval by any regulatory agency worldwide. We also impart Onsite GMP Training and also perform on site Process or Method Validation Studies.

Good Manufacturing Practice (GMP)

These guidelines are laid down with the intention of providing minimum requirements that a pharmaceutical or a food product manufacturer must meet while manufacturing drugs or food products ,which then assures that the products manufactured/produced are of high quality and do not pose any risk to the consumer or public.
  • Good manufacturing practice guidelines provides guidance for manufacturing, testing, and quality assurance in order to ensure that drug product is safe for human consumption.
  • GMP guidelines are not prescriptive instructions on how to manufacture products. They are a series of general principles that must be observed during manufacturing.
  • When a company is setting up its quality program and manufacturing process, there may be many ways it can fulfill GMP requirements.

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