Compliance Manager

Organize and Track your Compliance Evidence with Countries.

Regulations, Guidance, Standards, Technical Documentation, Procedures, and much more.
With Dashboards, Compliance Status Trackers, Comments, Related Reviews, Tasks, and much more.
 
Organize, manage and track your compliance evidence with ready-to-use and up to date global templates for assessments, checklists and more.
 
Ready to use templates for 225+ Countries related to Regulations, Guidance, Essential Principles, MDSAP, Audit preparations, Declarations, and much more. Export when you need it in our preferred formats.
 
Stay compliant and on top, keep in existing or go to new countries, explore new requirements faster, with ready to use templates and AI support, embedded with the latest news of MedBoard Search and MedBoard Intelligence.
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Make the Most out of MedBoard

Discover our Software Products for Regulatory Needs and Professionals:

Access to up to date Regulatory Intelligence, data, tools and News in more than 225 Countries, organized, curated and cleaned by MedBoard.
With a coverage of 15+ regulatory areas, including MedTech, Pharma/BioTech and Clinical trials, that includes countries curated summaries for an unparallel research and intelligence.

Add Documents and Standard that apply to your organization to the Compliance Manager! 

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Review systematically Regulatory News and Updates connected to our Global Data covering 225+ countries and 15+ regulatory areas in real time. Customize it, create protocols, impact assessments, actions, and reports easily with MedBoard.

The Compliance Manager is seamlessly integrated with your Review Process: you can access the outcome of the Impact Assessment of a Document at any time through Related Reviews.

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The Task Manager integrates with MedBoard data and modules to easily action, track, and complete efficiently any task and project by teams and professionals. Customize your workflow, and view your projects as a Task List or Board View. Easy to use, with intuitive UI to help you get started fast.

Create Tasks & Action, and connect them to your Document Portfolio to implement any required action.

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A powerful ready-to-use Products Information Management to organize, manage and track information about your products, product codes, SKUs, and its information, including Unique Identifiers (e.g. UDI), all integrated together with Regulatory Intelligence and MedBoard Search. 

Link your Regulatory Documents, Standards, Technical Documentation, and Procedures to your Products Codes and Families.

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A powerful ready-to-use Country Registrations RIMS to organize, manage, and track information about your countries registrations, certificates, licenses and economic operators, all integrated together with Regulatory Intelligence, Regulatory Reviews, Task Manager and MedBoard Search.

Link your Regulatory Documents, Standards, Technical Documentation, and Procedures to your Registrations, Certificates, License, Operators, and more.

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All modules integrate seamlessly with each other,
to keep all connected, in one place.

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