FDA, Good Manufacturing Practices GMP, quality system QSR, ISO 13485 regulatory consultants manufacturing development device, drug, diagnostic, combination medical products, 510(k), PMA, IDE

The Tamarack Group

The Tamarack Group is an association of consultants who provide US and international regulatory approval and compliance advice for the development and commercial production of medical products.

We are experts in regulatory approvals, quality systems and GMPs, organizational management, product and process development, risk management, verification and validation, facility requirements and qualification, clinical trial design and evaluation, commercial manufacturing and testing, and post-market feedback. We offer a full range of services by maintaining professional liaisons with other industry experts in areas such as statistics, validation, clinical trial management, and toxicology/material biocompatibility.

The Tamarack Group was established to offer our unique combination of scientific knowledge and industry insight to help you maintain compliance and compete in today's complex global markets.

Click here to view our full list of consulting services.