asertain™ filter validation services are specially designed to comprehensively meet international regulatory requirements. These are well supported by stringent Quality Management Systems which include validated test methods and calibrated measuring and testing equipment and auditable data generation and help establish functionality, testability and compatibility of sterilizing grade filters with the drug product.

Why choose us?

• Short lead times: 6-8 weeks after receipt of drug sample and protocol  approval
• Regulatory support
• State-of-the-art labs ensure high accuracy and data reliability
• Detailed and structured reports to comply with different regulatory requirements

Download Brochure for more details.