Suppliers / Nanjing King-Friend Biochemical Pharmaceutical

Nanjing King-Friend Biochemical Pharmaceutical

China 10 employees Updated 9 July 2026

Nanjing King-Friend Biochemical Pharmaceutical is a contract manufacturer based in China. It holds 2 active US drug master files across a filed portfolio of 2 molecules. Its filings concentrate with NPRA (MY), EDE (AE) and ARCSA (EC). Its GMP standing is certified by ANVISA (Brazil), MHRA (UK) and US FDA, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 14 March 2025 as NAI.

2
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
18
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
6 of 6 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 14 March 2025 NAI US FDA
  • 23 March 2018 NAI US FDA
  • 15 May 2015 VAI US FDA
  • 21 December 2012 VAI US FDA
  • 21 October 2010 NAI US FDA
  • 4 September 2009 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Nanjing, United Arab Emirates Not on file
Nanjing, United Arab Emirates Not on file
NANJING, China Not on file
NANJING, China Not on file
China, China 3004664441

What they file, and where

Molecule Regulators Docs
Enoxaparin US FDA 1
Heparin Sodium US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 12 None
EDE (AE) 2 None
ARCSA (EC) 2 None
JFDA (JO) 1 None
UZPHARM (UZ) 1 None
ANVISA (Brazil) None 3
MHRA (UK) None 3
US FDA None 1
EMA None 1

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Open risk flags

  • The most recent inspection outcome was NAI, on 14 March 2025.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates