Pharmaceutical Industry Course
This course offers practical guidance on launching generic oral solid dosage forms, covering GMP, regulatory compliance, bioequivalence, quality management, supply chain, validation, serialization, packaging, logistics, and team coordination for safe and effective product launches.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Pharmaceutical Industry Course provides a straightforward, hands-on guide to launching a generic oral solid dosage form on the market with assurance. You will learn basics of GMP, regulatory files, bioequivalence, and quality management, then progress to obtaining APIs and excipients, validating processes, preparing for inspections, applying serialization, handling packaging, logistics, and coordinating team efforts for launching safe, compliant, and effective products.
Elevify advantages
Develop skills
- GMP & quality systems: apply GMP, QC testing, and CAPA in actual generic manufacturing setups.
- Regulatory dossiers: prepare CTD, DMF, and ANDA documents for generic approvals.
- Tech transfer & validation: assist in scaling up, PPQ, and verifying processes.
- Supply chain & sourcing: evaluate API/excipient suppliers and ensure steady material supply.
- Serialization & logistics: set up packaging, track-and-trace systems, and cold-chain management.
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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