Global Certificate in Regulatory Affairs Documentation Writing
-- ViewingNowThe Global Certificate in Regulatory Affairs Documentation Writing course is a comprehensive program designed to meet the growing industry demand for expertise in regulatory affairs documentation. This course emphasizes the importance of accurate and compliant documentation in the medical device, pharmaceutical, and biotechnology industries.
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Kursdetails
⢠Regulatory Affairs Fundamentals
⢠Global Regulatory Documentation Requirements
⢠Good Documentation Practices in Regulatory Affairs
⢠Writing Regulatory Submissions (eCTD, NeeS)
⢠Regulatory Writing for Clinical Trials (Protocols, IBs, CSRs)
⢠Labeling and Package Inserts for Global Markets
⢠Regulatory Writing for Pharmacovigilance (PSURs, DSURs)
⢠Regulatory Intelligence and Literature Searching
⢠Quality Management in Regulatory Documentation Writing
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