Products and Services

1. Medical Writing Software 6/17/2025

   Accelerate Medical Writing Without Compromising Accuracy or Compliance

   In the fast-paced world of clinical research, the ability to produce, review, and finalize high-quality documents—on time and with full regulatory compliance—is non-negotiable. Ideagen Document Review (formerly known as PleaseReview) is the trusted collaboration and co-authoring platform that enables clinical teams to streamline document reviews, reduce version chaos, and ensure traceable, auditable feedback across the board.

2. Delivering High-Quality Patient Outcomes Data 9/16/2025

   Delivering high-quality patient outcomes data with patented technology, rapid deployment, and expert guidance.

3. Distribute, Monitor, And Exchange Study Documents With Every Site 6/12/2025

   Effortlessly distribute, monitor, and exchange study documents with every site—wherever they work, whenever they need it.

   Other tools promise site connections, but they can't deliver 100% coverage with a solution sites actually want.

   Adoption

   They claim sites use their tool…but you need sites to love it.

   Tracking

   They let you send documents…but you need to know the status of every document at every site.

   Integration

   They offer integration within their ecosystem…but you need compatibility with every site and sponsor software.

4. Document Review Integrations And Technology Partners 6/18/2025

   At Ideagen, we're committed to empowering seamless collaboration and enhancing your document review process. Through strategic alliances with leading technology providers across the life science industry, we offer integrations that amplify the efficiency and effectiveness of your workflows.

5. Clinical Trial Recruitment Reinvented 12/17/2024

   Clinical Site Services (CSSi) is the industry leader in delivering strategic patient recruitment and enrollment solutions to study sites, sponsors and CROs.

6. The SaaS Clinical Data Science Platform 4/8/2024

   Signals Clinical streamlines clinical data workflows, reducing the time spent preparing data for analytics. Its comprehensive platform enables the rapid delivery of clinical insights that inform both clinical and operational study decisions.

7. Drug Development Experience For Biotechs 8/8/2024

   Leverage our extensive expertise across over 120 therapeutic indications to drive your success.

8. Safety And Pharmacovigilance In-House Services 7/31/2024

   Clinical trials safety monitoring and reporting is vital to ensure participant safety, data integrity and regulatory compliance.

9. Clinical And Regulatory Strategy 11/7/2023

   Many biotechnology companies come to Australia to conduct early phase clinical trials and take advantage of straightforward regulatory streams and of the lucrative 43.5% R&D cash refund scheme. Biotechnology companies then often look at locations in Asia, such as South Korea, Thailand and China to tap into their huge treatment-naïve patient populations for their later phase clinical research.

10. Castor-eCOA Clinical Trial Technology 8/21/2025

    1,735 eCOA & ePRO Studies Completed 

    eCOA and ePRO with Enrollment, eConsent, Payments and EDC integrated. Our services cover build, licensing and 24/7 support.

    95%+ Patient Compliance Rate

    4-8 Weeks to Deploy

    190+ Validated Instruments