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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 straightforward, hands-on guide to launching a generic oral solid dosage form on the market with assurance. You will learn basics of GMP, regulatory files, bioequivalence, and quality management, then progress to obtaining APIs and excipients, validating processes, preparing for inspections, applying serialization, handling packaging, logistics, and coordinating team efforts for launching safe, compliant, and effective products.

Elevify advantages

Develop skills

  • GMP & quality systems: apply GMP, QC testing, and CAPA in actual generic manufacturing setups.
  • Regulatory dossiers: prepare CTD, DMF, and ANDA documents for generic approvals.
  • Tech transfer & validation: assist in scaling up, PPQ, and verifying processes.
  • Supply chain & sourcing: evaluate API/excipient suppliers and ensure steady material supply.
  • Serialization & logistics: set up packaging, track-and-trace systems, and cold-chain management.

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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