“Our regulatory affairs team saved quite a bit of time by having one centralized source to go to for global regulations and requirements.”

Director of Regulatory Affairs,
Medium-Sized Medical Company

RegDesk Regulatory Intelligence

Every journey begins with a single step. The most important step to introducing your medical products to new markets is initial intelligence gathering. RegDesk saves time and reduces risk by providing the most comprehensive, up-to-date regulatory intelligence on the web. Global medical device registration requirements are condensed into easy-to-follow steps and translated to English when necessary.

 

Benefits of Using RegDesk Regulatory Intelligence

  Instant Access to Global Regulatory Requirements

Challenge:

Traditionally, gathering regulatory intelligence requires months of research. Industry consultants can provide insight but are often slow to respond due to a high volume of inquiries or their own lack of knowledge about individual products or region-specific requirements.

Solution:

Regdesk provides instant access to comprehensive regulatory requirements for more than 115 countries. Our platform eliminates months of waiting , endless email chains and in-person meetings by giving you all the information you need at the click of a mouse.

  Up-To-Date Requirements

Challenge:

Global regulations constantly change, placing companies who rely on old intel from past research at increased risk of application rejection.

Solution:

Our analysts continuously monitor the global medical device regulatory landscape and update our intelligence when requirements change. The regulatory requirements we provide are the most accurate and updated regulatory information on the web.

  Regulatory Requirements that are Easy to Understand

Challenge:

Regulatory requirements provided by national agencies are often filled with jargon, esoteric wording, and ambiguous classification descriptions. Translations to English are often poorly executed.

Solution:

Medical device registration guidelines provided by our platform are synthesized into easy-to -follow checklists and translated to English when necessary. We give you the information you need to move forward confidently with your application.

Why Choose US

The medical device industry is evolving quickly in response to recent innovations in communications and data processing technology. Relying on search engines or industry consultants to gather regulatory intelligence is as old-fashioned now as relying on print publications seemed ten years ago. Now is the time to adopt new solutions to age-old problems like expanding to foreign markets.

Speak to a Regdesk Expert today!

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