Suppliers / Savior Lifetec

Savior Lifetec

Taiwan Updated 9 July 2026

Savior Lifetec is an API manufacturer based in Taiwan. It holds 4 active US drug master files across a filed portfolio of 4 molecules. Its filings concentrate with MINSA (CR), ARCSA (EC) and NMPA (CN). Its GMP standing is certified by EMA, ANVISA (Brazil) and US FDA, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 23 October 2025 as VAI.

4
active US DMFs
0
valid CEPs
6
registered plants 1 with an FDA FEI number
6
filings across 3 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

  • 23 October 2025 VAI US FDA
  • 29 November 2022 VAI US FDA
  • 26 October 2018 VAI US FDA
  • 22 April 2016 VAI US FDA
  • 16 May 2014 NAI US FDA
  • 13 May 2011 VAI US FDA

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

Registered plants

Site FDA FEI
MIAOLI COUNTY, Taiwan Not on file
MIAOLI, Taiwan Not on file
TAINAN, Taiwan Not on file
Tainan City, Taiwan Not on file
Tainan City, Taiwan Not on file
Taiwan, Taiwan 3005840211

What they file, and where

Molecule Regulators Docs
Imipenem SFDA (Saudi Arabia), US FDA 3
Cilastatin SFDA (Saudi Arabia), US FDA 2
Meropenem SFDA (Saudi Arabia), US FDA 2
Ertapenem SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Cilastatin API Ertapenem contract manufacturing Imipenem API Meropenem contract manufacturing Paliperidone contract manufacturing Prucalopride contract manufacturing

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 3 None
ARCSA (EC) 2 None
NMPA (CN) 1 None
EMA None 4
ANVISA (Brazil) None 1
US FDA None 1
MHRA (UK) None 1

Questions about Savior Lifetec

Does Savior Lifetec hold a US DMF or a CEP?
Savior Lifetec holds 4 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 Savior Lifetec FDA-registered?
One site operated by Savior Lifetec 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 Savior Lifetec's last inspection go?
The most recent inspection on record closed on 23 October 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 6 inspections are on file.
Where does Savior Lifetec manufacture?
6 registered sites are on record, in Taiwan (Miaoli County, Miaoli and Tainan among others). Every site is listed on this page with the register it came from.
What does Savior Lifetec make?
4 molecules are on record against Savior Lifetec, including Imipenem, Cilastatin, Meropenem and Ertapenem. Each links through to that molecule's full manufacturer list.
Which regulators recognise Savior Lifetec's GMP?
Current GMP certificates are on record from EMA, ANVISA (Brazil), US FDA and MHRA (UK). 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.

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Open risk flags

  • The most recent inspection outcome was VAI, on 23 October 2025.

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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