Pharmaceutical Industry Course
This course equips participants with essential knowledge and skills for launching generic oral solid dosage forms, covering GMP, regulatory compliance, bioequivalence, quality management, supply chain, validation, serialization, packaging, logistics, and cross-functional coordination for safe and efficient market entry.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Pharmaceutical Industry Course provides a clear, practical guide to launching a generic oral solid dosage form on the market with assurance. You will learn GMP basics, regulatory submissions, bioequivalence, and quality management, then advance to procuring active ingredients and excipients, validating processes, preparing for inspections, implementing serialization, handling packaging, managing logistics, and coordinating cross-functional launch plans for safe, compliant, and efficient products.
Elevify advantages
Develop skills
- GMP & quality systems: apply GMP, QC testing, and CAPA in real generic plants.
- Regulatory dossiers: prepare CTD, DMF, and ANDA files for generic submissions.
- Tech transfer & validation: support scale-up, PPQ, and process verification.
- Supply chain & sourcing: qualify API/excipient vendors and secure material flow.
- Serialization & logistics: implement packaging, track-and-trace, and cold-chain.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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