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, and cross-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 onto the market with assurance. You will cover the basics of GMP, regulatory submissions, bioequivalence, and quality management, then progress to procuring active ingredients and excipients, validating processes, preparing for inspections, implementing serialisation, handling packaging, logistics, and coordinating cross-team efforts for launching safe, compliant, and effective products.
Elevify advantages
Develop skills
- GMP & quality systems: apply GMP, quality control testing, and corrective actions in actual generic manufacturing facilities.
- Regulatory dossiers: compile CTD, DMF, and ANDA documents for generic drug approvals.
- Tech transfer & validation: assist with scaling up production, process performance qualification, and verification.
- Supply chain & sourcing: evaluate suppliers of APIs and excipients to ensure steady material supply.
- Serialisation & logistics: set up packaging, track-and-trace systems, and temperature-controlled distribution.
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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