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German consultant for the pharmaceutical industry.
Consulting firms specializing in supporting hospitals, physicians and attorneys address complex coding issues. Major emphasis on working with counsel in support of fraud and abuse allegations from third-party payers.
Their employee development solutions provide for compliance management and learning management; our Gxp compliance Edition is "validation ready", ideal for GxP compliance training requirements in the pharmaceutical or medical device industries.
European pharmaceutical/biotech consultancy specializing in project management, medical writing, and business development.
Regulatory affairs consultancy headquartered in North Carolina.
A resource for issues surrounding the FDA's 21 CFR Part 11 Rule on electronic records and signatures.
Medical Device RA and Quality System Consultants
Regulatory, quality and technical affairs guidance for international medical diagnostic device manufacturers.
Consultant Group specializing in providing services on FDA Compliance Issues to the Food, Drug and Cosmetic industry.
21 cfr part 11 regulatory compliance of FDA pharmaceutical GMP validation for ERP life sciences computer information systems.