Boost Your Knowledge of Global Regulatory Requirements for Your Specific Products

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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

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 an artificial intelligence (AI) platform that provides medical device companies regulatory intelligence for over 50 countries in real-time.

Q: How can I use RegDesk Dash?

A: Simply login to your dashboard, select your product and country and get instant access to regulatory knowledge.

Q: How soon can I see the requirements for my product?

A: Depending on the plan you choose, the information can be made available instantly.

Q: Who updates the information on the platform and how often?

A: RegDesk’s system updates the platform in real-time. As and when a market updates the requirements for your product, you can soon see it on your dashboard.

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

A: Yes, invite as many colleagues as you desire form across your organization. Boost collaboration across your global team and improve efficiency of your regulatory team.

Q: Can my team use RegDesk Dash to collaborate and learn?

A: Yes! We encourage teams to upload their knowledge to the dashboard to share with the global team.

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

A: Pricing depends on the package you selectClick here.

Q: Do you have any special pricing for startup companies?

A: Yes! Please contact us at desk@regdesk.co to learn about our Startup Package.

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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