Suppliers / Lifecore Biomedical

Lifecore Biomedical

United States 279 employees Updated 9 July 2026

Lifecore Biomedical is an API manufacturer based in United States. It holds one active US drug master file.

1
active US DMFs
0
valid CEPs
1
registered plants
4
filings across 1 regulators

Registered plants

Site FDA FEI
Chaska, United Arab Emirates Not on file

What they file, and where

Molecule Regulators Docs
Hyaluronic Acid US FDA 1

Also appears on these molecule pages

Hyaluronic Acid API

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 4 None

Questions about Lifecore Biomedical

Does Lifecore Biomedical hold a US DMF or a CEP?
Lifecore Biomedical holds 1 active US drug master file. 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.
Where does Lifecore Biomedical manufacture?
1 registered site is on record, in United Arab Emirates (Chaska). Every site is listed on this page with the register it came from.
What does Lifecore Biomedical make?
1 molecule is on record against Lifecore Biomedical, including Hyaluronic Acid. Each links through to that molecule's full manufacturer list.
Where does Lifecore Biomedical file?
Filings are on record with EDE (AE), 4 in total.

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