SUBMIT YOUR GLOBAL APPLICATIONS FASTER.

ELIMINATE REDUNDANCY OF
EFFORT WITHIN YOUR REGULATORYTEAM.

Learn More About RegDesk Dash

Benefits of Dash

Save time on back and forth with your regional teams trying to collect regulatory intelligence
Beat your competition by preparing better applications faster
Open collaboration with your global Regulatory Affairs team
Track all your products globally through a state-of-the-art dashboard
Eliminate spreadsheets and disparate systems

Benefits of Dash

Save time on back and forth with your regional teams trying to collect regulatory intelligence
Beat your competition by preparing better applications faster
Open collaboration with your global Regulatory Affairs team

Access to RegDesk Dash is as simple as…

Identify your products

Select the Market(s)

Access regulatory requirements

Frequently Asked Questions

Q: What is RegDesk Dash?

A: RegDesk Dash is a smart (artificial intelligence enabled) medical device registration software that provides companies a centralized tool to prepare dossiers faster, track status of all products globally, and access synthesized regulatory requriements for 60 markets.

Q: How can I use RegDesk Dash?

A: You can access various tools by logging into your RegDesk Dash Dashboard.

Q: Who updates the regulatory intelligence on the platform and how often?

A: RegDesk updates the platform. As and when a market modifies or updates the requirements for your product, you can see it reflected on your dashboard.

Q: Can I invite my team members to see the dashboard?

A: Yes, invite as many regulatory colleagues as you desire form across your organization. Eliminate the use of spreadsheets and disparate systems. Collaborate with your global team.

Q: How much does RegDesk Dash cost and what markets can I use it for?

A: Pricing depends on the package you select. Contact us at desk@regdesk.co for details.

Have any other questions?

Featured Post

New Record Keeping Requirements for Clinical Trial Institutions for Medical Devices in China

The Chinese Food and Drug Administration (CFDA) is the regulatory body in China that oversees the safety and efficiency of foods, pharmaceuticals, medical devices, and cosmetics. The CFDA recently issued regulations to enforce record-keeping of clinical trial institutions for medical devices. The new regulations will go into effect on January 1, 2018. The CFDA issued …

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