Trial Design Solutions

  1. The Importance Of Patient Recruitment In Clinical Trials 3/28/2025

    Why Patient Recruitment Matters in Clinical Research

    Patient recruitment is one of the most critical aspects of a clinical trial’s success. Without an adequate and diverse participant pool, trials risk failing to generate reliable and representative data. Ensuring sufficient participation is essential for producing statistically valid results that confirm the treatment's safety and effectiveness.

    For biotech companies, especially those under tight timelines and budgets, partnering with an experienced CRO like Novotech ensures that patient recruitment efforts are both efficient and effective, enabling timely trial completion and robust data collection.

  2. IRB Review Services For Phase I Research 12/22/2021

    With experience overseeing thousands of Phase I studies in the US and Canada, Advarra’s institutional review board (IRB) understands the unique requirements of Phase I study design and conduct. Our dedicated team and processes are built to support your Phase I research needs.

  3. NextGen Participant Engagement Platform 11/16/2023

    Uncover how the GreenSpace platform can address delays in trial timelines by overcoming insufficient recruitment and retention efforts.

  4. Recruit Patients Faster In The Asia-Pacific Region 9/29/2022

    Novotech relies on years of experience, in-country knowledge and real-life big data to identify and propose the best-performing sites and investigators for your study.

  5. Expert Travel Solution For Clinical Trial Participants 7/15/2019

    Getting participants to and from a research site can be burdensome for the site staff, study coordinators, participants, and their families and/or caregivers. Greenphire has designed the most comprehensive travel solution built to meet the retention goals of global clinical research.

  6. Improve eTMF Document Processing Speed And Quality

    In any eTMF — at any stage — ensure timely, right-first-time processing from source to archive with help from Phlexglobal leadership in TMF best practices.

  7. Phlexglobal Experts Fill The Gaps In eTMF Management 12/16/2022

    Enable busy study teams to assess, prevent, and manage risk across the entire TMF spectrum – improving inspection-readiness with less effort.

  8. Strategic Advising For Lifecycle Development: Navigating Complexity With Precision 5/15/2024

    Discover tailored strategies crafted to align with your company's goals and objectives that draw upon extensive past, present, and ongoing experiences to drive success at each pivotal stage of your journey.

  9. Your Top Partner For Ophthalmic Drug Development 4/9/2024

    As a leading partner in ocular therapy, Altasciences is at the forefront of ophthalmic drug development. Our integrated CRO/CDMO solutions can support your program from lead candidate selection to market. You will benefit from working with a single partner as your product advances through each phase of drug development—from prototype formulation through preclinical testing, to early phase clinical trials, and manufacturing. This could mean up to 40% in time savings.

  10. Home Trial Support: The Engine Powering DCT 8/10/2021

    By conducting trial visits outside of the site, physicians can expand their reach, making drug development more accessible. Read about how MRN's Home Trial Support "HTS" is the engine powering DCTs.