Pharmaceutical Industry Course
Master the full lifecycle of generic oral solid drugs—from GMP, quality control, and regulatory dossiers to tech transfer, serialization, and supply chain—so you can drive safe, compliant, and profitable launches in today’s pharmaceutical industry.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
This Pharmaceutical Industry Course gives you 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 move through sourcing APIs and excipients, process validation, inspection readiness, serialization, 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.
- Serialization & logistics: implement packaging, track-and-trace, and cold-chain.
Suggested summary
Before starting, you can change the chapters and 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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Course in PDF