Event
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:
- QC analysts
- R&D scientists
- R&D managers
- Regulatory affairs specialists