Ben Venue Laboratories' Quality Policy

By fully understanding our jobs and work procedures, we will provide products and services conforming to mutually agreed customer requirements.

Because we are a contract pharmaceutical manufacturer, Ben Venue is inspected by global healthcare authorities. These inspections include FDA Pre-Approvals and over 50 annual audits by our customers. These customers are from many different enforcement districts of the FDA, giving us an overall picture of cGMP trends and changes in cGMP requirements. Additionally, our facility is inspected by international regulatory authorities for customers of Ben Venue wishing to distribute into world markets.

The company is dedicated to strict cGMP compliance and the methods, facilities and controls used for the manufacture, processing, packing and holding of all finished pharmaceuticals produced at BVL are in accordance with the applicable sections of cGMP regulations. A continuing employee training program, equipment and process validation, and a self-inspection program are part of the company's Total System Control approach to quality assurance. The entire company is committed to an ongoing Quality Improvement Process. Special emphasis is placed on thorough documentation and review of the entire manufacturing and control process. The documentation system and customized batch documents assure that requirements have been met. These documents are reviewed and updated as necessary to maintain quality standards.