Register entry

CIS BIO INTERNATIONAL

Data as of · How to read this entry

Registered sites
1
Active NDC listings
0
Live patents
0
Countries
1
Base
France
Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Finished drug manufacture1Packaging1sterilize1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
CIS Bio InternationalRegistrant: CIS BIO INTERNATIONALRTE NATIONALE 306, SACLAY, ILE DE FRANCE 91400, France (FRA)Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture, Packaging, sterilize1000268008381560168
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Common questions

Is CIS BIO INTERNATIONAL FDA approved?
CIS BIO INTERNATIONAL holds 1 FDA-registered establishment in France. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are CIS BIO INTERNATIONAL's drugs manufactured?
The FDA register lists SACLAY. Registered operations: analytical testing, active ingredient (API) manufacture, finished drug manufacture, packaging, sterilize.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.