Are you looking for a targeted course for your professional development?
If you are interested in a single module or more than one, you are in the right place!
We have compiled the individual modules of the course in GMP Guidelines & Quality Assurance Overview and turned them into a course specific to your needs.
Our specialist courses
that will help you on your career path.
Our courses will enable you to put your new knowledge into practice immediately.
The pharmaceutical industry and GMP Guidelines
Get acquainted with the basics of GMP standards, the pharmaceutical industry and its departments right away and you will find your way around the company much easier!
- How do you work in GMP compliance environments?
- Classification of the main areas and departments
- GMP regulations: key concepts
- Terminologies, acronyms and definitions
- Roles and responsibilities in Quality Assurance, Quality Control, Production and Warehouse Departments.
A two-hour course with always-on content and interactive quizzes to study:How do you work in GMP compliance environments?
- Classification of the main areas and departments
- GMP regulations: key concepts
- Terminologies, acronyms and definitions
- Roles and responsibilities in Quality Assurance, Quality Control, Production and Warehouse Departments.
GMP Documentation
Knowing the regulatory requirements for documentation is essential for anyone working with Pharmaceutical Quality. Want to learn more? You are in the right place!
Always available ondemand content, two hours of video lessons and exercises to study:
- Batch Record Review & Batch Release
- The role of the Qualified Person (QP)
- Annual Product Review
Process & Cleaning
Validation
Do you want to learn more about Process and Cleaning Validation in the pharmaceutical sector? This ondemand course will provide you with a comprehensive and clear overview!
- The principles of Quality by Design (QbD)
- Basic concepts of Process Validation
- Basic concepts of Cleaning Validation
Deviations &
Change Control
Do you want to learn more about Deviations, Non-Conformities and all the unforeseen issues you may have to deal with in a pharmaceutical company? Here is the perfect course for you.
Two hours of video to watch whenever you want, with quizzes and slides, to learn more about
- Change Control System
- Deviation Management
- Corrective And Preventive Actions (CAPAs)
- Out of Specification (OOS)
- Out of Trend (OOT)
Training Management, supplier Audits and Self Inspections
Pharmaceutical training, self-inspections, supplier audits. Three key topics for every QA Specialist. If you want to learn more, this is the course for you!
Thanks to interactive and always available content and two hours of video lessons that you can watch whenever you want, you will learn deeper:
- Training Management System
- Self-Inspection Management
- Audit ai fornitori