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Regulatory Compliance

European CE Marking,


Technical Files,


US FDA 510(k) Clearance,


US PMA Approvals


Canadian Medical Device License

 

Canadian/US FDA Establishment License

 

 

 

 

 

 

 

Quality System Compliance

 

US FDA GMP And Quality System Regulation


ISO 13485 Consulting (With/Without CMDCAS)


Canadian Medical Device Requirements (CMDCAS)


FDA 483 Response,


Internal And Supplier QMS Audits,


QA/QMS Compliance Services

 

Other Services

 

Corporate/

employee Training

 

Medical Device Validation Consulting (including software)

 


ISO 14971 Consultants for Medical Device Risk Management

 

ISO/IEC 17025

 

Environmental management

 

 

MORE!

 
 
 
 

Medical Device Consulting

Located in the Toronto, Ontario (Canada) region, Regulatory Progress Associates (RPA) are experts in the field of Medical Device Regulations and the processes that govern their sale in many regions including: USA, Canada, Europe, Latin America and Australia. We offer outstanding customer support at very affordable prices. Whatever your challenges, we will help you through. Ask us through our FREE no-obligation quote today.

Whether you are looking simply for advice, or require a temp employee to fill in a gap, RPA can help. 

 
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Our Mission
 
We will guide you through your most challenging obstacles while providing the very best in service! 

 
     
     
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