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 Date: 2013-07-03 04:36:11Evaluation Standards Quality Pharmaceutical industry Validity ISO/IEC 17025 Good Clinical Laboratory Practice Validation Good Laboratory Practice Quality management Technology Science |
| The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia has prepared the unofficial consolidated text for the Medicinal Products Act which includes: Medicinal Products Act (Official GazetteDocID: 1r1yj - View Document |
| Code of Practice for the Promotion of Animal Medicines Together with the Rules of Procedure for theDocID: 1q2Fu - View Document |
| IRIS PHARMA FACT SHEET A GLOBAL SERVICE PROVIDER OF PRECLINICAL AND CLINICAL RESEARCH IN OPHTHALMOLOGY KEY FACTS COMPANY OVERVIEWDocID: 1pBzr - View Document |
| Rules on the Medicines ActDocID: 1p48T - View Document |
| R: Regulatory Compliance and Validation Issues A Guidance Document for the Use of R in Regulated Clinical Trial Environments December 15, 2014DocID: 1lWkU - View Document |