Application Notes & Case Studies

  1. Defining And Implementing Global Data Standards & Governance 10/28/2024

    Discover how implementing global data standards and governance for a biopharma company, creates unified data management, standardized terminology, and a central ontology to enhance R&D efficiency.

  2. Drug Development Program Management 10/28/2024

    Learn how a consultant helped a biotech company specializing in immuno-oncology to develop timeline reports for the product and portfolio and identify and address gaps in the filing plan.

  3. Transforming Patient Support For A Multinational Pharmaceutical Company 10/23/2024

    As part of an expansion project, a large multinational pharmaceutical company sought a partner to simplify the payment and travel processes, improving their patients' experience.

  4. Improving Patient Health And Safety: SOPs And Process Mapping 10/21/2024

    In this study, a biotech company faced compliance challenges due to inadequate SOPs that lacked detailed process maps. Propharma stepped in to provide a strategy and project plan.

  5. Successful Special Procedure Study Conduct: Cerebrospinal Fluid (CSF) And Concurrent Muscle Biopsy 10/17/2024

    Worldwide assisted a trial sponsor with a study exploring a novel therapeutic protein (TP) in 48 healthy volunteers.

  6. Partnering For Precision In An IPF Study: Securing Timely Deliverables And Key Endpoints 10/17/2024

    A pharmaceutical company enlisted Worldwide Clinical Trials to help achieve on-time results for their Phase IIa IPF clinical trial, enabling them to manage vendors and meet challenging deadlines.

  7. Muscular Dystrophy: Multi-National And Multi-Site Trials 10/15/2024

    Learn about the success ReveraGen found when expanding their partnership with Novotech to a larger phase 2b trial (VBP15-004) in Duchenne Muscular Dystrophy (DMD).

  8. Using eConsent Data To Populate Site And Sponsor Data Systems 10/7/2024

    A top-10 pharmaceutical company was looking to reduce the amount of administrative burden on their clinical trial sites and themselves. See how we accomplished it, using eConsent.

  9. Flexible Integrations To Reduce Risks And Increase Efficiencies 10/4/2024

    Learn how a trial team kept the blind of central lab samples and patient treatment across a Phase III and extension trial, whilst optimizing the supply chain.

  10. Complex Randomization Delivered Successfully 10/4/2024

    Learn about the strategy and successful execution of a complex randomization design that helped LG Chem overcome its clinical trial challenges alongside eClinical randomization experts.