An extensive overview of clinical pharmacology, drug development, and regulatory affairs, focusing heavily on the scientific and ethical considerations in bringing new medicines to market. The text explores the specifics of various drug types, including traditional chemicals, biologicals, advanced therapy medicinal products (ATMPs), and orphan drugs, detailing their unique development challenges. Key topics include pharmacokinetics (PK) and pharmacodynamics (PD), the importance of clinical trial design (e.g., randomization, blinding, and observational studies), and the critical role of pharmacogenetics and biomarkers in personalized medicine. Furthermore, the sources cover crucial regulatory aspects like bioequivalence for generics and biosimilars, drug reimbursement, pharmaceutical drug safety (pharmacovigilance), and the ethical framework governing clinical research (e.g., the Declaration of Helsinki and ICH-GCP).
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