Pharmaceutical Industry Course
Gain expertise in the complete lifecycle of generic oral solid drugs, covering GMP, quality control, regulatory dossiers, tech transfer, serialization, and supply chain management to ensure safe, compliant, and profitable product launches in the pharmaceutical sector.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course offers a practical guide to launching generic oral solid dosage forms. Master GMP basics, regulatory dossiers, bioequivalence, quality systems, API and excipient sourcing, process validation, inspection readiness, serialization, packaging, logistics, and cross-functional launch strategies for compliant and efficient products.
Elevify advantages
Develop skills
- GMP and quality systems: apply GMP, QC testing, and CAPA in generic plants.
- Regulatory dossiers: prepare CTD, DMF, and ANDA for generic submissions.
- Tech transfer and validation: support scale-up, PPQ, and process verification.
- Supply chain and sourcing: qualify API and excipient vendors and secure materials.
- Serialization and 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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