Obesity Services & Products

  1. A Single Digital Experience Participants Will Love 8/29/2024

    Experience higher data quality, retention and participant compliance by providing a truly engaging experience from data submission to reminders, appointment management, telemedicine and more -- from the phone, tablet, or desktop.

  2. Manufacturing And Import License (MIA) And Batch Certification 8/29/2024

    Navigating both the specific country and general European regulations and requirements to supply medicinal products to the European markets can be a complex challenge. This applies both to Marketing Authorisation Holders (MAH) of approved commercial medicinal products and Sponsors of clinical trials.

  3. Patient Support And Commercial Services 8/29/2024

    Global solutions tailored for your unique needs.

  4. Functional Service Provider (FSP) 8/29/2024

    At ProPharma, we offer a unique approach to the traditional Clinical Research Organization (CRO) Full-Service Provider (FSP) model.

  5. Flow Cytometry Services 8/27/2024

    Experience customized and validated flow cytometry (FCM) biomarkers and panels for your clinical research on a global scale. Learn how FCM can enhance your research and help develop the panels you need.

  6. R&D Technology 8/22/2024

    Technology solutions for life sciences that get products to market quickly and efficiently.

  7. Medical Information 8/22/2024

    25 years of Providing World-Class Medical Information Services.

  8. Pharmacovigilance Services And Solutions 8/22/2024

    Industry leading pharmacovigilance solutions from clinical development through post-approval.

  9. Quality And Compliance 8/22/2024

    Compliance solutions for product development agility and audit readiness.

  10. 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.