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Pharmaceutical Industry Course

Pharmaceutical Industry Course
flexible workload of 4 to 360h
valid certificate in your country

What will I learn?

This course offers a practical guide to launching generic oral solid dosage forms. It covers GMP basics, regulatory filings, bioequivalence studies, quality management, API and excipient sourcing, process validation, inspection preparation, serialization, packaging, logistics, and team-based launch strategies for compliant and efficient products.

Elevify advantages

Develop skills

  • GMP and quality systems: Implement GMP, QC testing, and CAPA in generic drug plants.
  • Regulatory dossiers: Prepare CTD, DMF, and ANDA submissions for generics.
  • Tech transfer and validation: Handle scale-up, PPQ, and process verification.
  • Supply chain and sourcing: Qualify API and excipient vendors for steady supply.
  • Serialization and logistics: Set up packaging, track-and-trace, and cold chain.

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.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor of the Prison System, and the course from Elevify was crucial for me to be chosen.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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