stadmin July 22, 2022 No Comments MARKETING APPROVAL of MEDICINAL PRODUCTS: Regulatory procedures & applications Registration and maintenance procedures during the life cycle of medicinal products: Centralized, DCP, MRP, National. registration applications eCTD Your name Your email Phone number Select the training ROLE & RESPONSIBILITIES OF PHARMACOVIGILANCE LOCAL CONTACT PERSONINTRODUCTORY COURSE - KEY CONCEPTS AND PROCESSES IN PHARMACOVIGILANCEQualification and validation of GxP IT systemsQuality Risk management in GxP areaQualification and periodical evaluation of GxP suppliersQuality Management Systems for the Pharmaceutical Industry - Fundamental Concepts. Practical aspects.REGULATORY AFFAIRS INTRODUCTORY COURSE – MEDICINE LIFE CYCLEGPD course – Management of non-conformities related to distributed products (medicines, food supplements, medical devices)REGULATORY AFFAIRS INTRODUCTORY COURSE - THE ROLE OF REGULATORY AFFAIRS PROFESSIONALS IN DRUG PRODUCTS LIFE CYCLEGood Distribution Practice. Compliance with Current Regulations – Requirements, Implementation.DISTRIBUTION OF MEDICINAL PRODUCTS, MEDICAL DEVICES AND FOOD SUPPLEMENTS in European Union (EU) Practical approach for implementation of regulatory (GDP) requirements, by Contract Giver and Contract AcceptorMARKETING APPROVAL of MEDICINAL PRODUCTS: Regulatory procedures & applications Your message (optional) I agree with the data processing policy
