Level 4: Licensed Medicines Manufacturing & Regulation
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Level 4: Licensed Medicines Manufacturing & Regulation

£299.00

  • Expert-level guide to UK/EU licensed medicine production
  • Learn about MHRA, EMA, GMP, MA, and pharmacovigilance
  • Ideal for those entering the licensed pharma sector
  • In-depth guidance on documentation and licensing processes
  • Trusted by QA managers, pharmacists, and manufacturers
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Description

Level 4 of the SKD Academy Series offers an advanced and technically detailed guide to the licensed pharmaceutical sector. This course manual is ideal for professionals transitioning from supplements to medicines, or for manufacturers aiming to understand MHRA and EMA frameworks. You’ll learn how to prepare for a Marketing Authorisation (MA), implement GMP and GDP systems, and operate within the legal structures of the pharmaceutical supply chain.

Topics include QP oversight, pharmaceutical licensing routes, pharmacovigilance, serialization, and facility inspection readiness. Whether you’re involved in tablet production, importation, or compliance, this level gives you real-world insight into running a fully compliant licensed medicine operation.

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