Pharmaceutical Industry Course
This course offers practical guidance on launching generic oral solid dosage forms, covering GMP, regulatory compliance, bioequivalence, quality management, API sourcing, process validation, inspections, serialization, packaging, logistics, and team strategies for compliant 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 into the market with assurance. You will cover GMP basics, regulatory submissions, bioequivalence, and quality management, then proceed to procuring APIs and excipients, process validation, preparing for inspections, serialization, packaging, logistics, and team-based launch strategies for safe, compliant, and effective products.
Elevify advantages
Develop skills
- GMP & quality systems: implement GMP, QC testing, and CAPA in actual generic manufacturing setups.
- Regulatory dossiers: compile CTD, DMF, and ANDA documents for generic approvals.
- Tech transfer & validation: assist with scaling up, PPQ, and process confirmation.
- Supply chain & sourcing: vet API/excipient suppliers and ensure steady material supply.
- Serialization & logistics: set up packaging, track-and-trace systems, and cold-chain handling.
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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