MDC has more than 25 years varied experience in all aspects of medical device consultancy.
The MDC Team always provides good value for money consultancy from very experienced professionals who are recognised as excellent at what they do. No one knows it all, but good team work and mutual support provides for very comprehensive, effective advice and assistance with implementation.
It’s because of this we are able to efficiently get you through the complex regulatory compliance process whilst transferring skills and developing both your business and your people.
We add real value to your business by providing:
- Strategic business reviews & planning, marketing, research and product management from concept to market.
- Partner search and selection services.
- Regulatory training and assistance to help you achieve compliance to requirements in the United Kingdom (UKCA)
- Regulatory training and assistance to help you achieve compliance to requirements in the European Union (CE marking).
- Regulatory training and assistance to help to achieve compliance to United States (US) Food and Drug Administration (FDA) requirements.
- Pragmatic Quality Management System (QMS) development for starts-up through to multinationals that meet international standards.
If you’d like to know more about how our expertise can enhance and reinforce your medical device projects, please contact us here.