Ranked API manufacturers
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for foetal bovine serum, filing since 2023.
Last FDA inspection
Not established
GMP recognised in
Not established
Holds one valid CEP for foetal bovine serum, filing since 2024.
Last FDA inspection
Not established
GMP recognised in
Not established
03 United States
Makes the API
Credentials confirmed against the regulator files on 25 July 2026
Holds 3 valid CEPs for foetal bovine serum, filing since 2024.
Last FDA inspection
Not established
GMP recognised in
Not established
04 United States
Makes the API
Credentials confirmed against the regulator files on 25 July 2026
Holds 2 valid CEPs for foetal bovine serum, filing since 2007.
Last FDA inspection
Not established
GMP recognised in
Not established
05 United States
Makes the API
Credentials confirmed against the regulator files on 25 July 2026
Holds 3 valid CEPs for foetal bovine serum, filing since 2021.
Last FDA inspection
Not established
GMP recognised in
Not established
Holds one valid CEP for foetal bovine serum, filing since 2006.
Last FDA inspection
Not established
GMP recognised in
Not established
Credentials confirmed against the regulator files on 25 July 2026
Holds 2 valid CEPs for foetal bovine serum, filing since 2008.
Last FDA inspection
Not established
GMP recognised in
Not established
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for foetal bovine serum, filing since 2023.
Last FDA inspection
Not established
GMP recognised in
Not established
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for foetal bovine serum, filing since 2025.
Last FDA inspection
Not established
GMP recognised in
Not established
6 more manufacturers hold filings for foetal bovine serum
The names are listed below. The filings, inspection history and GMP certificates behind
each one are available with a free account.
Open the full list with a free account How this list is built
The order is set by active filings weighted by regulator, inspection outcomes and their
recency, breadth of GMP recognition, and evidence of real exports, less any open risk flags.
Every factor appears on the card it produced.
Read the full method.
- Active US DMFs
- FDA, List of Drug Master Files
- Valid CEPs
- EDQM certificate database
- Inspection outcomes
- FDA inspection classifications
- GMP certificates
- EudraGMDP and national regulators