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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 course offers a practical guide to launching generic oral solid dosage forms. Master GMP basics, regulatory dossiers, bioequivalence, quality systems, API and excipient sourcing, process validation, inspection readiness, serialization, packaging, logistics, and cross-functional launch strategies for compliant and efficient products.

Elevify advantages

Develop skills

  • GMP and quality systems: apply GMP, QC testing, and CAPA in generic plants.
  • Regulatory dossiers: prepare CTD, DMF, and ANDA for generic submissions.
  • Tech transfer and validation: support scale-up, PPQ, and process verification.
  • Supply chain and sourcing: qualify API and excipient vendors and secure materials.
  • Serialization and logistics: implement packaging, track-and-trace, and cold-chain.

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.
Workload: between 4 and 360 hours

What our students say

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

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