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About

RegDesk is a Regulatory Information Management System (RIMS) that helps medical device companies manage global regulatory submissions, product registrations, and compliance in one centralized platform. It streamlines regulatory workflows, organizes regulatory data, and provides global regulatory intelligence to help teams navigate complex requirements across multiple markets. Regulatory affairs and quality teams benefit by reducing manual work, improving submission accuracy, and accelerating time to market. Our capabilities are as follows: • AI Application Builder • Regulatory Intelligence • Change Assessment • Standards Management • Country-Specific Templates • Distributor Collaboration • AI Document Management • Tracking & Reporting • Alerts and Notification • Product Management • Claims Management • EUDAMED For more information, visit our website.

About

End-to-end regulatory information management on a single platform. The Vault RIM Suite streamlines global regulatory processes on a single, cloud-based platform, enabling life sciences companies to improve visibility, data quality, and agility. Respond faster to changing regulations and increase process efficiency from submission planning to publishing. Coordinate regulatory efforts across HQ, affiliates, and partners within a single RIM system. Ensure teams are developing reliable regulatory content with high data integrity. Veeva Vault Registrations manages product registration data worldwide, including registration status, variations, and health authority interactions. Veeva’s flexible data model accommodates IDMP data points and will continue to support evolving regulatory data standards. Veeva Vault Submissions streamlines submission planning through approval by automating regulatory process steps.

Platforms Supported

Windows Not Supported
Mac Not Supported
Linux Not Supported
Cloud Supported
On-Premises Not Supported
iPhone Not Supported
iPad Not Supported
Android Not Supported
Chromebook Not Supported

Platforms Supported

Windows Not Supported
Mac Not Supported
Linux Not Supported
Cloud Supported
On-Premises Not Supported
iPhone Not Supported
iPad Not Supported
Android Not Supported
Chromebook Not Supported

Audience

Medical Devices, Pharmaceuticals, and IVD companies

Audience

Companies in need of an end-to-end regulatory information management platform to streamline global regulatory processes

Support

Phone Support Supported
24/7 Live Support Not Supported
Online Supported

Support

Phone Support Supported
24/7 Live Support Not Supported
Online Supported

API

Offers API Not Supported

API

Offers API Not Supported

Screenshots and Videos

Screenshots and Videos

Pricing

Contact us to learn more.
Free Version Not Supported
Free Trial Not Supported

Pricing

No information available.
Free Version Not Supported
Free Trial Not Supported

Reviews/Ratings

Overall 5.0 / 5
ease 5.0 / 5
features 5.0 / 5
design 5.0 / 5
support 5.0 / 5

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Pros & Cons from Real Users

Pros

  • Comprehensive, user-friendly tool that consolidates all regulatory affairs processes in one place. Excellent support provided by real experts that add value to our business.
  • The User Interface is very elegant and engaging to use. The Global view of Alerts, Standards and Regulations is appealing and consolidated and is a useful tool for regulatory intelligence.
  • RegDesk is easy to deploy, entirely web-based with streamlined user access management. Its UI is intuitive which makes training users simple. Its modular structure reduces complexity for folks working on specific topics, which may not relate to the work of another colleague -- for example, Regulatory Intelligence and market access requirements appear in one module, while tracking submissions is in another. Additionally, tracking postmarket "where-can-I-ship?" elements is simple and straightforward with a SKU and country-code database.
  • Compliance is critical in the medical device world to ensure safety of users and patients. Compliance tracking allows companies to establish and maintain a validated state of control, while looking at efficient ways to stay ahead of changing regulations. Documentation Management allows organizations to prepare for future growth by reviewing content from multiple dossiers and leverage similarities of content increase speed to submission. In many situations’ documents are updated as products progress through lifecycle and by managing documentation change electronically increases efficiency. Utilizing reporting and statistics during business planning allows Regulatory Affair heads to show organizations the return on investment for regulatory departments. Reporting on the number of requests, submissions, approved/cleared submissions and timelines allows key performance indicators to be develop. Being able to report on the number of international requests allowed for the organization to enhance their approach on global expansion. Easy to implement and utilize, customization and collaboration with RegDesk team, tracking to allow for reporting to organizations allowing for visibility of global changes/updates.

Cons

  • There are no cons so far. The company was able to make small adaptations to our routine.
  • Some features are not available for general users, like importing data and reporting. The vendor's technical team was able to assist us with these requests.
  • My firm's use case is slightly different than what most RegDesk customers would be looking for, however the team were highly responsive in clarifying our needs and then engaging with additional experts to add the regulatory intelligence information we had requested. This did take a little bit of time up front, but the RegDesk team were professional and very supportive.
  • No cons come to mind, RegDesk is exceptional in the collaboration with organizations.

Training

Documentation Supported
Webinars Supported
Live Online Supported
In Person Supported

Training

Documentation Supported
Webinars Not Supported
Live Online Supported
In Person Supported

Company Information

RegDesk
Founded: 2014
United States
www.regdesk.co

Company Information

Veeva
United States
www.veeva.com/products/vault-rim/

Alternatives

Alternatives

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Rimsys

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Rimsys

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Rimsys Regulatory Management Software
Redica

Redica

Redica Systems
Veeva Vault

Veeva Vault

Veeva Systems
Freya

Freya

Freyr Solutions
Ennov RIM

Ennov RIM

Ennov
RIMTrack

RIMTrack

WinWire Technologies

Categories

Categories

Integrations

5X Not Supported
Active Directory Supported
Arena Supported
Asana Supported
Boomi Supported
Dynamics 365 Customer Service Supported
Freu AI Not Supported
Indent Not Supported
Jira Supported
MuleSoft Anypoint Platform Supported
Okta Supported
OpenText AI Operations Management Supported
Oracle ADF Faces Supported
PTC Windchill Supported
Qualio Supported
Resource Management by Smartsheet Supported
SnapLogic Supported

Integrations

5X Supported
Active Directory Not Supported
Arena Not Supported
Asana Not Supported
Boomi Not Supported
Dynamics 365 Customer Service Not Supported
Freu AI Supported
Indent Supported
Jira Not Supported
MuleSoft Anypoint Platform Not Supported
Okta Not Supported
OpenText AI Operations Management Not Supported
Oracle ADF Faces Not Supported
PTC Windchill Not Supported
Qualio Not Supported
Resource Management by Smartsheet Not Supported
SnapLogic Not Supported
Claim RegDesk and update features and information
Claim RegDesk and update features and information
Claim Veeva Vault RIM and update features and information
Claim Veeva Vault RIM and update features and information