Any facility involved in production of a bio/pharmaceutical product has a significant impact on the quality of the end products it manufacturers. To certify the safety and effectiveness of these products, regulatory agencies require testing to monitor and validate the on-line and off-line performance of the manufacturing process to ensure the appropriate process control procedures are in place.
As a pioneer in the Microbiology, Chemistry, Biochemistry and Biosafety testing for more than 25 years, Eurofins Lancaster Laboratories offers a comprehensive range of services to help drug manufacturers achieve compliance through a variety of process validation tests, including:
- Bioprocess Residuals
- Viral Clearance
- Facility Monitoring and Support
- Cleaning Validation and Disinfectant Efficacy Studies