MDCPartners helps manufacturers of medical devices and IVD’s to obtain regulatory approval to market products throughout Europe. We assist with a broad spectrum of regulatory issues to support and maintain compliance. MDCPartners can take some of the burden off your RA/QA department or coach the selection and implementation of the optimal regulatory pathway. Navigating the CE marking process, preparing your certification audits, or identifying and monitoring the global standards landscape that applies to your specific situation, our advice and/or hands-on support is tailored to the scale and scope of your company. MDCPartners has created normScan, a web-based standards tracking tool tailored to your product range
Our services for device manufacturers
See also
normScan
Regulatory advice and CE marking process support
Standards compliance support
European Authorized Representative for Medical Devices and IVDs
MDCPartners provides tools and services that assist pharmaceutical companies make better decisions. Whether optimizing study placement or selecting research partners, or managing your portfolios. Our technologies coupled with our experience bridge many information gaps. Our flagship product called ta-Scan is a new technology class; a living system which monitors and aggregates internet information. We scan disclosure, corporate and regulatory websites and create powerful ontologies that classify research relationships.
MDCPartners offers many issue based services. We report comprehensive intelligence utilizing our technologies which enable real time snap shots of development cycles and market environments.
More on our pharmaceutical consultancy services
See also
ta-Scan
What does ta-Scan do?
Issue based consultancy for the pharmaceutical sector
Collaborative information to enhance global project feasibility
Marketing Insights and Reports for Life-Cycle Management
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