Regémon is a consulting and training firm assisting medical device and biotechnology companies in the area of quality, regulatory compliance and clinical services.

Enjoy the benefits of external regulatory and compliance support to provide a specific expertise or to manage workload during personnel shortages or high workload situations.

Regémon provides support throughout product lifecycle: from concept/ feasibility and product design/ development through post-market compliance.  Our short- and long-term strategies ensure an efficient product development program and timely product approvals.

Our services are focused on assisting small and mid-size companies achieve regulatory compliance with FDA, European, Canadian and Japanese regulations:

• Obtaining Pre-market approvals (510(k), PMA, EU Technical Files/ Design Dossiers)
• Implementing compliant systems and processes (FDA QSR, CE Marking, ISO 13485, MDD, AIMD, CMDR, ISO 9001)
• Staying in compliance (audits, training, FDA reporting)
• Resolving regulatory problems (Crisis Management) – FDA audit response (483), warning letters, and product recalls 

We provide practical solutions and work with you to develop and implement effective regulatory strategies, prepare domestic and international regulatory submissions, manage FDA and foreign regulatory agencies inspections and train your employees in all aspects of regulatory compliance.

Offices in:  USA (San Antonio, Texas) and Europe (Hamburg, Germany)