stadmin July 22, 2022 No Comments

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 Acceptor

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    ROLE & RESPONSIBILITIES OF PHARMACOVIGILANCE LOCAL CONTACT PERSON
    • ROLE & RESPONSIBILITIES OF PHARMACOVIGILANCE LOCAL CONTACT PERSON
    • INTRODUCTORY COURSE - KEY CONCEPTS AND PROCESSES IN PHARMACOVIGILANCE
    • Qualification and validation of GxP IT systems
    • Quality Risk management in GxP area
    • Qualification and periodical evaluation of GxP suppliers
    • Quality Management Systems for the Pharmaceutical Industry - Fundamental Concepts. Practical aspects.
    • REGULATORY AFFAIRS INTRODUCTORY COURSE – MEDICINE LIFE CYCLE
    • GPD 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 CYCLE
    • Good 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 Acceptor
    • MARKETING APPROVAL of MEDICINAL PRODUCTS: Regulatory procedures & applications

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