Partnering Solutions

31. Translational And Biomarker Sciences: Enabling Breakthroughs 5/2/2025

    Learn about expert services specializing in precision medicine and biomarker-driven contract and clinical research that can assist you through translational solutions.

32. Advancing Development And Approval Of Rare/Ultra-Rare Disease Therapies 5/8/2024

    Veristat empowers rare disease therapy with science-driven strategies and trusted expertise, supporting over 350 rare disease projects and preparing 40+ marketing applications in the past five years.

33. Your Partners In Drug Development And Safety 2/11/2025

    How can Ergomed use its oncology expertise, global reach, and access to patients with rare and ultra-rare diseases can help your organization achieve efficient, high-quality clinical trial execution?

34. Central Nervous System Drug Development 3/4/2021

    Our expert central nervous system (CNS) teams have extensive experience and strong knowledge of the challenges expected when implementing and mitigating CNS clinical trials.

35. Solutions For Sponsors: Power Remote Cardiac Monitoring In Your Clinical Trials 11/19/2024

    At the Forefront of Cardiac Monitoring Solutions

    Transforming ECG technology in clinical trials

36. Why IQVIA Participant Payments? 10/30/2024

    Learn about how this participant-friendly technology ensures efficient and secure payments, enhancing the clinical trial experience for all involved.

37. 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).

38. The Next Generation Of Oral Targeted Therapies 8/11/2025

    Solve the unique challenges of poorly soluble molecules like targeted protein degraders (TPDs), such as PROTACs and molecular glues, seamlessly accelerating your molecule from development to commercialization.

39. Clinical Trial Regulations 4/11/2025

    This essential guide walks through mastering the complex landscape of clinical trial regulations, providing a clear, practical breakdown of regulatory timelines, legal obligations, and more.

40. Site Management And Clinical Monitoring 5/28/2024

    Our experienced Regional Site Managers (RSMs) are recapturing the importance of building relationships with clinical sites. Our RSMs can act as a “one-stop shop” for all activities related to a clinical study site.