CLS MedPharma’s GMP approved testing facility works in partnership with leading manufacturers of Medical Devices and Pharmaceutical products.
CLS’s Medpharma is managed by senior experienced personnel who understand the industry. CLS has invested in state of the art facilities and technology to deliver the most up to date and appropriate solutions to their clients. For CLS this ensures that they continue to work in partnership with leading companies and for their clients this helps to ensure they support their current products and help create their future business and next generations of products.
CLS MedPharma provides GMP approved Analytical Chemistry and Microbiology testing using Compendial test methods /Customer specific test methods, ICH /FDA Guidelines or relevant ISO Standard. In addition, its capability includes stability storage and subsequent testing as per ICH guidelines and also includes provisions for performing batch release testing and subsequent QP release as per EEC Directive 75/319/EEC.
CLS continues to offer strategic supports to their cleanroom and pharmaceutical clients by providing sampling, testing and product release services.
CLS Medpharma supports and works in partnership with the following:
- Medical Device Manufacturers
- Biotechnology Companies
- Hospitals (Sub group’s operating theatres, chemo, IVF,
- Bloodbank, & Maintenance)
- High Risk Industries