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Pharmaceutical Industry Course

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

What will I learn?

This Pharmaceutical Industry Course provides a clear, practical guide to launching a generic oral solid dosage form on the market with assurance. You will learn GMP basics, regulatory submissions, bioequivalence, and quality management, then advance to procuring active ingredients and excipients, validating processes, preparing for inspections, implementing serialization, handling packaging, managing logistics, and coordinating cross-functional launch plans for safe, compliant, and efficient products.

Elevify advantages

Develop skills

  • GMP & quality systems: apply GMP, QC testing, and CAPA in real generic plants.
  • Regulatory dossiers: prepare CTD, DMF, and ANDA files for generic submissions.
  • Tech transfer & validation: support scale-up, PPQ, and process verification.
  • Supply chain & sourcing: qualify API/excipient vendors and secure material flow.
  • Serialization & logistics: implement 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 the chosen one.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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