Partnering Solutions

  1. Integrated Programs To Bridge Molecules From Discovery Into Clinical Development 1/4/2023

    A new collaboration helps to remove obstacles from the critical path, reduce development risks, eliminate the white space in pre-clinical drug development, and shorten the pathway to clinical development.

  2. Data Integrity Drives Every Step Of Your Clinical Trial 9/17/2025

    Choose the right Data Sciences team to save time without compromising quality. Find out what sets us apart, from comprehensive strategies to cutting-edge solutions.

  3. IQVIA Learning Management System 5/20/2020

    IQVIA’s Learning Management System (LMS) provides sites and study teams with a single, efficient source for education and learning, knowledge assessments, reporting and more.

  4. RegOps Services To Streamline Regulatory Submissions 5/28/2024

    Our RegOps team offers document-level publishing or management of the entire regulatory submission process. Coupled with our electronic document management system (Veeva), we can oversee all technical aspects for submission of your dossier (eg, eCTD document granularity, utilization of content templates, document formatting, hyperlinking, bookmarks, navigation, publishing, and redaction services).

  5. Quality Assurance Services 7/31/2024

    The quality assurance (QA) team ensures the highest standards from pre-clinical to market by focusing on operational quality control, quickly identifying potential issues, and implementing necessary changes.

  6. Greenphire Travel 10/24/2025

    With dedicated coordinators and multilingual staff worldwide, Greenphire ensures smooth, compassionate travel experiences — removing barriers to participation and enhancing trial accessibility.

  7. Biometrics 4/28/2021

    Advancing a novel therapy through clinical development is complicated. Not all therapies make it to the patients that need them.

  8. Greenphire Clinical Finance: Budgeting & Benchmarking 10/23/2025

    Streamline trial budgets and payments with real-time fair market data, speeding startups and ensuring timely, transparent site funding worldwide.

  9. Suite Success For CROs 9/13/2021

    Shorten start-up times for your research studies by eliminating manual spreadsheets once and for all. SuiteSuccess for CROs allows you to unify clinical applications to improve visibility and oversight across the organization.

  10. Early Development: Accelerating Molecules Through To Proof-Of-Concept 3/3/2022

    Our integrated approach brings together drug substance, drug product and clinical activities, supporting the expediting of lead molecules from FIH into POC trials.