We provide GMP service as per FDA QSR to worldwide customers

  • Medical Device 21 CFR 820
  • Finished Pharmaceutical Formulation 21 CFR 211
  • Dietary Supplements 21 CFR 111
  • Finished Food 21 CFR 110

GMP guidelines are not clear cut instructions on how it should be and how to manufacture products. They are a series of general principles that must be observed during manufacturing, storing, testing, transportation and marketing.

The service of an experienced consultant having wide knowledge and experience will benefit, by providing step by step guidance how to follow GMP.

We provide Gap assessment and Internal Audits for

    • FDA Pr-Inspection.
    • FDA Post- Inspection.
    • FDA compliance assessment Audit
    • GAP Assessment
    • FDA 483 Closing

Hurry !, send your enquires, we like to serve you enquiry@meddevicecorp.com