Regulatory News Systematic Reviews

Perform proactive regulatory monitoring and impact assessments in a systematic, easy, and integrated process.

Customize 225+ Countries and 15+ Regulatory areas to your needs. Use MedBoard software, automations, workflows, integrated intelligence, and AI-powered features, to produce compliant regulatory reviews faster, with more precision and more cost-effective.

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Real Time

Powered by MedBoard Global Data, get automatic updates and notifications in real-time from Authorities News based on your criteria.

Customizable

Customize your review framework for a consistent process shaped to your needs. Apply systematic reviews to many databases.

Connected

Connected with other MedBoard solutions such as Intelligence, Compliance Manager, Products Information or Countries Registrations.

Audit Trail

Show the evidence that you keep track and review updates, whether it is for internal use, customers, or for Authorities.

Easy to Use

Connected with other MedBoard solutions such as Compliance Manager, Products Information or Countries Registrations.

Secure

Your privacy and security are our top priority. MedBoard is ISO 27001 certified, ensuring robust information security management.

"Definitely a really great platform to use. It's like having an online work colleague helping me in my role."
Sonia Newton
Regulatory Affairs Associate, Inotec AMD

Say Goodbye to manual processes


Features that automate your workflow
 and minimize your manual work

 

Customize your monitoring and appraisal

Authorities’ News and Standards Updates

Customize MedBoard real-time regulatory databases to your needs, including Authorities News and Standards Lifecycle Updates and Adoptions. 

225+ Countries

Select the countries that apply to you and use filters and queries. 

15+ Regulatory Areas

Select the sectors that apply to you, including MedTech, Pharma, Clinical Trials, AI, and many more.

Configure your Appraisal Criteria

Fully customizable appraisal plan for Impact Assessments with custom questions, scores and extraction tables, adapted to your needs.

"I feel more confident that I am not missing anything, and it is easier to see the big picture"
Yaara Yarmut
Chief Regulatory Officer, Alimetry

Changes evaluation, impact assessments and actions

Email Notifications

Get automatic updates and notifications in real-time from Authorities News based on your search plan and strategy.​

Fast Screening

One-click screening on an easy to use interface supported by filters, sub-searches, custom filters, and many more features.

Full Review and Impact Assessment

Embedded Review Assessment Card for each update, side-by-side PDF viewer, custom questions and many more features.

MedBoard AI Analyzer

Use the MedBoard AI Analyzer to extract from regulatory documents key information, regulatory requirements, summaries, and documents cited.

Task Manager

Ensure implementation with an integrated project management solution to assign reviews, collaborate, and create tasks, actions and deadlines.

"Duplication of work has been minimized between excel tracking sheets and actions now that we have all the capabilities of systematic review."
Kylie Marflak
Senior Regulatory Intelligence Specialist, CooperVision

Reporting

Report your reviews

Report instantly the outcomes of your review within a period, relevant items impacting the company, review progress with visual flowcharts, and impact assessments evaluations. 

Export data, appraisals and analytics

Export data, flowcharts, appraisals and analytics linked to your review. Our reporting options are fully customizable and adapt to any filter selection.

Transfer regulatory items to Compliance Manager automatically

Seamlessly integrated with the MedBoard Compliance Manager, transfer relevant documents directly from your Systematic Review and add them to your compliance scope.

100%

CSAT

Customer Satisfaction (CSAT) Score,
with an average overall satisfaction with MedBoard of 4,8/5.

50%

Reduced Manual Work

86% of MedBoard users report reducing
by more than 50% the need for
manual actions and work.

3x-10x

Faster Processes

78% of MedBoard users reported
performing actions 3x to 10x faster,
accelerating their processes.

Customer Stories

GUERBET –  Pharmaceutical Manufacturer

 I have found its Regulatory Systematic Reviews process to be easily incorporated into our existing procedures. It is also very helpful for Regulatory preparation for Management Reviews

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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Organize, manage and track your compliance evidence with the Compliance Manager. This module helps to identify and control the specific regulations, guidance, standards, procedures, technical documentation that apply to you, and to organize, action, and track your related compliance evidence. 

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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.

Ready to Get Started?

Request a free demo today to see how MedBoard can transform your organization and teams