Curriculum
Course Description:
This course provides an overview of pharmaceutical industry and business values and effective use of USP General Chapters. Participants will be introduced to basic quality concepts and compliance as it pertains to quality culture, data integrity, laboratory working essentials, drug dosage types and forms, regulatory affairs and the International Council for Harmonization (ICH).
Upon completion of this course, you will be able to:
- Describe quality control structure in the pharmaceutical and business industries
Who Should Participate:
New recruits in he industry with at least 1 year of experience including:
- QC analysts
- R&D scientists
- R&D managers
- Regulatory affairs specialists
Access Duration:
Access to this course expires 60 days from the date of registration or until you mark the course ‘Complete’ – whichever occurs first.