Products and Services

  1. Strategic Regulatory Consulting & Planning 1/25/2024

    Applying experience, knowledge, and insights to plan and implement regulatory strategies for successful interactions with the FDA, MHRA, EMA, and other Global Regulatory Agencies.

  2. How ClinicReady Delivers Foundations For Success 8/8/2024

    ClinicReady is the surrogate for outsourced drug development team for preclinical biotechs.

  3. MRN Technologies 11/22/2024

    Our research is powered by MRN owned, regulatory-approved and validated eClinical software systems. Our technology can be used at-site and at-home enabling fully integrated data through any clinical trial.

  4. Clinical Operations And Project Management For Every Phase 12/21/2022

    Get streamlined and integrated clinical trial services delivered by a dedicated team of professionals with deep industry and therapeutic area expertise across all phases of clinical development. 

  5. Site And Patient Payments 12/5/2025

    With integrations at the heart of our efficiency model, Block Clinical automates payments in three areas: Site Payments, Patient Payments, and Supplier Payments.

  6. TrialKit eConsent 11/18/2024

    Help your patients make informed decisions without burying them in paper

    With electronic informed consent (eConsent) software, your patients can access consent forms using any device they choose. And because it’s part of TrialKit’s unified platform, both your patients and your study team get a seamless experience.

  7. NetSuite For The Biotechnology Industry 11/15/2024

    Biotech companies progressing through clinical trials, planning an IPO, and undergoing rapid growth have a unique set of financial, contract, compliance, and reporting needs. We have designed an ERP solution, built on NetSuite, to address all of these needs. With over 50 implementations in the last two years alone, SuiteSuccess for Life Sciences is quickly becoming the defacto software standard for all successful biotechnology companies.

  8. 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.

  9. Revvity Signals Software Risk-Based Monitoring Solution 8/28/2017

    The Revvity Signals Software Risk-Based Monitoring Solution is the most effective way to leverage data-driven insights to optimize site performance while improving patient safety.

  10. Central IRB Services 4/10/2025

    “Going the extra mile is a big part of our DNA. Personal attention can go a long way in ensuring the success of your next research study.”

    Raffaella Hart, MS, CIP
    Sr. Vice President, IRB and IBC Services

    Fast, reliable IRB review for multisite studies backed by expert oversight and responsive support. With streamlined submissions, frequent meetings, and dedicated client managers, BRANY IRB helps you save time and money while maintaining full regulatory compliance.