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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 onto the market with assurance. You will learn the basics of GMP, regulatory submissions, bioequivalence, and quality management systems, then progress to sourcing active ingredients and excipients, process validation, preparing for inspections, serialisation, packaging, logistics, and coordinated launch planning to ensure products are safe, compliant, and efficient.

Elevify advantages

Develop skills

  • GMP and quality systems: apply GMP, quality control testing, and corrective actions in actual generic manufacturing facilities.
  • Regulatory submissions: prepare Common Technical Document, Drug Master File, and Abbreviated New Drug Application for generic approvals.
  • Technology transfer and validation: assist with scaling up production, process performance qualification, and verification.
  • Supply chain and sourcing: evaluate vendors for active ingredients and excipients to ensure reliable material supply.
  • Serialisation and logistics: set up packaging, track-and-trace systems, and temperature-controlled distribution.

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 for 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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