Pharmaceutical Industry Course
This course offers a practical guide to launching generic oral solid dosage products, covering GMP, regulatory compliance, bioequivalence, quality systems, API sourcing, process validation, inspection readiness, serialization, packaging, logistics, and cross-functional launch planning for compliant and efficient market entry.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
This Pharmaceutical Industry Course provides a clear, practical roadmap to bring a generic oral solid dosage to market with confidence. Learn GMP fundamentals, regulatory dossiers, bioequivalence, and quality systems, then proceed through sourcing APIs and excipients, process validation, inspection readiness, serialisation, packaging, logistics, and cross-functional launch planning 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.
- Serialisation & 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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