Whether your product requires new analytical methods or analytical method optimization, PMI Bio can help. We establish custom product and process-specific strategies for obtaining reliable, scientifically sound results to ensure your pharmaceutical product is safe and effective.
PMI Bio supports these methods at each step of the drug approval process, throughout the analytical life cycle. Employing a wide range of analytical testing services and analytical equipment allows us to manage method transfer, optimization, qualification, and validation.
We also provide developmental stability services, including:
- Determination of stability-indicating methods
- Microbiological testing
- Pilot batch production and stability analysis
- Preformulation stability screens
- Stability storage and testing
“You can count on us for fast analysis and expert help with interpretation and decision making.”
BS in Chemistry
- 6 years industry experience in analytical chemistry, analytical QC, validations, and QA technical data review
- Specialties: Developing methods and performing validations for new client projects, support of routine release and stability testing, Karl Fischer titration, viscometry, and HPLC
- Passions: Family, travel, and her yellow lab, Hank