Specializing in the design, collection, and analysis of management information, business processes, and medical data for the pharmaceutical and biotechnology industries.
Assisting manufacturers of medical devices with Medical Device Directive regulatory compliance, including choosing an Authorized Representative to guide European Regulatory interests.
Independent consortium with manufacturing, packaging, marketing, distribution, and sales expertise seeking innovative, medically-based products to bring to the UK market.
UK based consultants to the pharmaceutical industry providing support and training in GMP, GLP, GDP, validation, auditing and regulatory compliance advice.
