Clinical Trials Products and Services

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

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

  2. Medical Writing: A Collaborative Approach 7/31/2024

    Discover how a collaborative approach to medical writing ensures the highest standards of excellence and precision in every document produced.

  3. Commercial/Clinical cGMP Quality Control Analysis 9/11/2024

    On-site labs with our own personnel offer greater control of samples and timelines, minimizing risk for our customers.

  4. Regulatory Sciences 8/22/2024

    We want your product to move through the regulatory process, gaining approvals and ultimately helping patients. Using our industry leading knowledge and skills, we will meet you where you are – gaining approval: for the first in human trials, in development, at scientific advice, at the end of phase 2, or post approval. At every level, our scientific expertise and in-depth knowledge of therapeutic backgrounds have guided every client we have to a successful outcome.

  5. Signal Management Services 8/2/2024

    ProPharma has deep expertise across all signal detection and management activities, including validation, prioritization, and assessment using data from a wide range of sources that are relevant for signal detection for the individual product(s). We are also fully trained and experienced in the EudraVigilance Data Analysis System (EVDAS) functionality and can support MAHs to comply with their obligations for signal detection and management. We leverage our robust knowledge to select the most efficient and effective method(s) for each product that is compliant with legislative requirements.

  6. Safety Assessment Services 6/20/2023

    A full range of in vivo and in vitro testing services that can be customized for your project’s needs to expedite preclinical development while maintaining a high quality standard.

  7. Advertising & Promotional Review Consulting 8/29/2024

    ProPharma has built the world’s leading and first full-service global solution dedicated to Advertising & Promotional Review. 

  8. Collect RWE With Natural History Studies 9/20/2023

    Developing a therapy for a rare or ultra-rare disease is life-changing work with unique challenges. Examine how natural history data is being used to inform the clinical development process.

  9. eCOA: Delivering High-Quality Patient Data 7/31/2025

    Purpose-built with users at the center to make it easier and more efficient to get quality patient outcomes data for submissions and approvals.

    Collecting quality data on patient outcomes is often one of the most important parts of a clinical trial. It is also challenging, and many eCOA solutions make it feel even more difficult with complicated processes, lack of questionnaire reusability, slow set up, and difficult to use tech.

  10. Quality And Compliance 8/22/2024

    Compliance solutions for product development agility and audit readiness.