With regulatory requirements, validation protocol, and data integrity all being in the forefront, it is important to equip the laboratory with more than just analytical equipment. By providing tools, resources and knowledge, PerkinElmer’s total solution approach to USP testing enables laboratories to be analyzing samples faster and ensures compliance with regulations on electronic records and signatures.
In this talk, we will discuss:
- USP Chapters 232 and 233 and ICH Q3D
- 21 CFR Part 11 requirements and compliance
- PerkinElmer’s offerings to streamline your elemental impurity testing
- Syngistix software to ensure data integrity and compliance
Target Audience
- Business Manager
- Clinical Trials Manager
- CRO Laboratory Manager
- Laboratory Manager
- Regulatory QA/QC
- Research Scientist
- Core Facility Manager
- Research & Development Manager
- Laboratory Technician
- Production/Process Manager
