Suppliers / Shenzhen Techdow Pharmaceutical

Shenzhen Techdow Pharmaceutical

China 2 duplicate records merged Updated 9 July 2026

Shenzhen Techdow Pharmaceutical is an API manufacturer based in China. It holds 2 active US drug master files. Its filings concentrate with Health Canada, ARCSA (EC) and INVIMA (CO). Its GMP standing is certified by EMA, MFDS (Korea) and ANVISA (Brazil). Its most recent recorded inspection, by US FDA, closed on 17 September 2019 as VAI.

2
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
34
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 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

  • 17 September 2019 VAI US FDA
  • 23 January 2015 NAI US FDA
  • 15 March 2012 NAI US FDA

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

Registered plants

Site FDA FEI
SHENZHEN, China Not on file
China, China 3005599762

What they file, and where

Molecule Regulators Docs
Enoxaparin US FDA 2

Also appears on these molecule pages

Enoxaparin API

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 13 None
ARCSA (EC) 12 None
INVIMA (CO) 3 None
EFDA (ET) 3 None
MINSA (CR) 2 None
UZPHARM (UZ) 1 None
EMA None 4
MFDS (Korea) None 2
ANVISA (Brazil) None 1

Questions about Shenzhen Techdow Pharmaceutical

Does Shenzhen Techdow Pharmaceutical hold a US DMF or a CEP?
Shenzhen Techdow Pharmaceutical holds 2 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Shenzhen Techdow Pharmaceutical FDA-registered?
One site operated by Shenzhen Techdow Pharmaceutical carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Shenzhen Techdow Pharmaceutical's last inspection go?
The most recent inspection on record closed on 17 September 2019 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file.
Where does Shenzhen Techdow Pharmaceutical manufacture?
2 registered sites are on record, in China (Shenzhen and China). Every site is listed on this page with the register it came from.
What does Shenzhen Techdow Pharmaceutical make?
1 molecule is on record against Shenzhen Techdow Pharmaceutical, including Enoxaparin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Shenzhen Techdow Pharmaceutical's GMP?
Current GMP certificates are on record from EMA, MFDS (Korea) and ANVISA (Brazil). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

Checking Shenzhen Techdow Pharmaceutical?

Ask Fred what the record holds on Shenzhen Techdow Pharmaceutical, including filings and inspection history.

Chat with Fred, your AI analyst
Opens WhatsApp. Free to start.

Open risk flags

  • The most recent inspection outcome was VAI, on 17 September 2019.

Comparable suppliers

Apitoria Pharma shares 1 molecule Gland Pharma shares 1 molecule Dongying Tiandong Pharmaceutical shares 1 molecule Hebei Changshan Biochemical Pharmaceutical shares 1 molecule Hubei Enoray Biopharmaceutical shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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