We specialize in Engineering, Validation, Regulatory, IT, and NON-IT related areas primarily focused on Pharmaceutical / Life Sciences and Medical devices, health care companies. About BCVS Global BCVS supports Pharmaceuticals, Biologics, Medical Devices, Combination Products, and Active Pharmaceutical Ingredients (API) to achieve the most cost-effective way to undertake their regulatory activities worldwide. This includes regulatory intelligence and strategy, worldwide product registration, preparation of regulatory documents, in country representation, establishment registration, and post-approval submissions. BCVS professionals possess a group of highly experienced professionals in validating medical device, pharmaceutical and biotechnology manufacturing processes. By partnering up with the Product Development, Supply Chain, R&D, Operations, Quality Assurance, Regulatory Affairs personnel, BCVS will ensure that all regulatory requirements and specifications are met. The Key to an effective Quality Management System (QMS) is to have your QMS aligned with your business needs. BCVS helps Pharmaceutical, Biotechnology; Medical Device companies achieve compliance with FDA, EMEA, ISO, and other recognized standards.