Trial Design Solutions

31. Reviewing Protocols Across Therapeutic Areas 2/5/2025

    A successful clinical trial starts with an efficient protocol review.

    With deep roots in academic research and clinical medicine, BRANY IRB is uniquely positioned to meet your cost and speed requirements. Get your clinical trial to the start line while ensuring participant health and safety.

32. Rare Disease Center Of Excellence Overcomes Unique Obstacles 7/14/2022

    Biorasi’s Beeline platform provides clinical teams with unique, real-time transparency for quick responses to rare and urgent disease trial challenges.

33. First In Human (FIH) Fact Sheet 1/26/2023

    Altasciences has decades of experience designing, conducting, and reporting on first-in-human (FIH) clinical trials. For small or large molecules, simple or complex trials, we have the expertise, purpose-built Phase 1 facilities, and seamless processes to deliver quality with speed and ease.

34. Ophthalmic Clinical Research Services 1/26/2023

    With over 40 clinical trials conducted in the area of ophthalmology, Altasciences combines depth of knowledge and expert capabilities to offer you a full range of early ophthalmic clinical development.

35. Only Elligo Mitigates Research Risk 4/18/2023

    Uncertainty is inherent in clinical research. Uncover new strategies and solutions to alleviate risk so clinical teams can confidently and quickly bring products to market.

36. Enable Your Clinical Trial Through Healthcare 11/13/2023

    Gain direct access to healthcare-first sites, elite research sites, and extensive site support, maximizing enrollment solution effectiveness for your clinical trials.

37. TrialScope Disclosure Management Brochure 9/24/2018

    TrialScope Clinical Trial Registry Manager (CTRM) delivers the proven solutions clinical trial sponsors need to centralize, track, register, and comply with clinical trial disclosure processes, mitigating compliance risks while giving them greater control over their own clinical trial disclosure reputation.

38. Recruitment Strategies: A Behind The Scenes Look 4/9/2025

    Explore a dynamic recruitment strategy being used to address the growing demand for participants in early-stage clinical trials while overcoming regulatory and ethical challenges.

39. Flexible And Simplified Consent Management 7/31/2025

    Learn about a unified ecosystem integrating eConsent, IRT, eCOA, and ePatient into a seamless workstream designed with a patient-centric approach.

40. Navigating The Use Of Controlled Substances In Clinical Trials Using IRT 8/20/2021

    Sponsor organizations that want to use controlled substances in clinical studies must manage the associated regulatory and logistical requirements. Read how this can be challenging for emerging biopharma.