ReadCube for Medical Affairs

Optimize Medical Literature Management and Monitoring for Strategic Decision-Making

Medical Affairs teams are tasked with staying informed on the latest clinical research, regulatory updates, and scientific developments to make data-driven decisions. ReadCube offers a complete solution for managing, organizing, and monitoring medical literature, helping Medical Affairs professionals access critical information quickly and efficiently.

Key Features for
Medical Affairs

comprehensive literature _ library

Centralized Literature Management for Clinical Data

Organize clinical studies, regulatory reports, and safety documentation in one easy-to-access library.

  • Categorize research by therapeutic area, drug, or study phase for easy retrieval.
  • Annotate and highlight key clinical findings for internal discussions or presentations.
  • Ensure that all teams have access to up-to-date materials, streamlining compliance and approval processes.
literature monitoring _ email alerts

Continuous Monitoring of Regulatory Changes

Stay current with the latest medical literature and regulatory developments by setting up customized alerts.

  • Automatically track new research in clinical trials, therapeutic areas, or drug safety.
  • Monitor regulatory updates to ensure your team remains compliant with the latest standards and guidelines.
  • Discover emerging trends and new treatment options that could inform strategy and decision-making.
cross functional collaboration _ add to lit review

Cross-Functional Collaboration and Knowledge Sharing

Facilitate collaboration across medical, clinical, and regulatory teams with shared libraries and insights.

  • Share key findings and annotated literature with teams to ensure alignment in decision-making.
  • Enable collaboration between Medical Affairs, clinical development, and regulatory functions, ensuring all teams have visibility into relevant data.

Benefits for Medical Affairs:

ReadCube’s scalable literature management solution makes it simple for you to build the library your organization wants to use. From custom workflows to automatic recommendations,  ReadCube is the literature management solution you’ve been waiting for.

Efficient Literature Management
Organize and categorize vast amounts of clinical and regulatory literature for easy access by your entire team.

Stay Compliant with Regulatory Changes
Monitor regulatory updates and ensure your team is always up to date with the latest standards.

Improve Decision-Making
Access the latest clinical data and trends to support strategic decision-making across medical affairs functions.

Responsible for staying informed on new clinical trial data and regulatory changes across a variety of therapeutic areas?

Using ReadCube, a Medical Affairs team sets up custom alerts to monitor key therapeutic areas and new clinical studies. Literature is organized by drug class and indication, allowing the team to quickly retrieve relevant information when preparing reports or presentations. 

By tagging important regulatory updates and clinical findings, they ensure compliance with the latest standards and can provide accurate, up-to-date data for medical decision-making. The result is faster, more informed responses to regulatory inquiries and internal strategy decisions.

By simplifying literature management and monitoring with ReadCube, you ensure that you have the most up-to-date clinical and regulatory information to make informed decisions. Stay compliant, informed, and aligned with the latest industry developments.

Schedule a demo

Fill out the form below to see firsthand what ReadCube can do for you and your team.
Name(Required)
Hidden
Location(Required)
How did you hear about us?
This field is for validation purposes and should be left unchanged.