USFDA Consulting Fees (CFR 820 & 510k)

We are providing various kind of US FDA related services, readers are requested to read appropriate pages mentioned below of correct information

If you are searching for US FDA Registration fees of Drugs, Food, Medical Device, Cosmetics, API and related services Please Click here

If you are searching for US FDA Drug Master File  submission and related fees, please click here

If you are searching for US FDA 510k Fees, please refer here

GMP / QSR implementation

If you are looking for support in GMP / QSR implementation related activities read the following details

Medical Device 21  CFR 820  related fees, Click Here

We are not providing GMP Implementation support as per 21 CFR 110 for packaged food and frozen food items

The US FDA Consulting we offer across the globe are the following:

  • QSR Implementation support
  • Documentation support
  • Training
  • Internal Audit / Quality Audit
  • Pre- audit before FDA auditors visit
  • Support during FDA auditors
  • Post audit support for closing NC/483

Please contact us for quick information.

INDIA – Bangalore
+ 91 994 591 2081
Phone / Viber / WhatsApp

USA – Chicago
+1 630 696 1293
Phone / Viber / WhatsApp


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