Drug Master Files for: Steris
✉ Email this page to a colleague
Steris Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10255 | A | V | 5/18/1993 | STERIS | CONTRACT STERILIZATION FACILITY IN WESTPORT MAYO, IRELAND |
10733 | A | V | 2/15/1994 | STERIS | CONTRACT STERILIZATION FACILITY IN MARSEILES, FRANCE |
11040 | A | V | 8/15/1994 | STERIS | CONTRACT STERILIZATION FACILITY IN DAVENTRY, UNITED KINGDOM |
13196 | I | V | 9/21/1998 | STERIS APPLIED STERILIZATION TECHNOLOGIES | CONTRACT STERILIZATION FACILITY IN GROVEPORT OHIO |
13237 | I | V | 9/28/1998 | STERIS ISOMEDIX SERVICES | CONTRACT STERILIZATION FACILITY IN TEMECULA,CALIFORNIA |
13238 | A | V | 9/28/1998 | STERIS APPLIED STERILIZATION TECHNOLOGIES | CONTRACT STERILIZATION FACILITY |
>DMF No. | >Status | >Type | >Submission Date | >Holder | >Subject |
Drug Master File Glossary
STATUS OF DMFS
- A = Active. This means that the DMF was found acceptable for filing, administratively, and is up-to-date.
- I = Inactive
- N = Not an assigned number
- P = DMF Pending Filing Review
TYPES OF DMFs
- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)
- Type II Drug Substance, Drug Substance Intermediate, and Material Used in Their Preparation, or Drug Product
- Type III Packaging Material
- Type IV Excipient, Colorant, Flavor, Essence, or Material Used in Their Preparation
- Type V FDA Accepted Reference Information