Suppliers / GE Healthcare (Shanghai)

GE Healthcare (Shanghai)

China 2 duplicate records merged Updated 9 July 2026

The public registers hold a second record for GE Healthcare (Shanghai). The fuller profile, with 13 active US DMFs and 4 valid CEPs, is at GE Healthcare. Figures on this page cover only this record.

GE Healthcare (Shanghai) is a finished-dose manufacturer based in China. It appears in 6 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with INVIMA (CO) and NPRA (MY). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
6
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Shanghai, China Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INVIMA (CO) 4 None
NPRA (MY) 2 None
EMA None 1

Questions about GE Healthcare (Shanghai)

Does GE Healthcare (Shanghai) hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for GE Healthcare (Shanghai). It does have 6 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does GE Healthcare (Shanghai) manufacture?
1 registered site is on record, in China (Shanghai). Every site is listed on this page with the register it came from.
Which regulators recognise GE Healthcare (Shanghai)'s GMP?
Current GMP certificates are on record from EMA. 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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Sources on this page

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