Newsletter | March 27, 2024

03.27.24 -- 4 Strategies To Accelerate Commercialization

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Unlock the key to seamless eCOA integration for your next clinical trial with IQVIA’s comprehensive Licensing Guide. From understanding licensing requirements to optimizing integration, our guide is your roadmap to streamlined eCOA implementation.

TRIAL MANAGEMENT

4 Drug Development Strategies To Accelerate Commercialization

Guest Column | By Mark Bleackley, Ph.D., Incannex Healthcare 

Given the extenuated clinical trial timelines, every chance to shave off time, save money, and obtain regulatory approval is one worth taking. Discover four ways to accelerate your therapy’s path to commercialization.

Pros And Cons Of Basing Clinical Trials In Today’s European Landscape

Article | Novotech

Explore the essential considerations for sponsors and CROs as they navigate the advantages and challenges of clinical trial locations, particularly in the United States and Europe.

Study Start-Up Challenges: Hard Realities, Effective Strategies

White Paper | IQVIA Technologies

Launching a study is complex, and the time between protocol approval and the first patient visit has increased dramatically. How can companies reverse this trend and accelerate study start-ups?

Trial Rescue: Leadership Approach To Propel Clinical Development

Case Study | By Rashida Challenger, Halloran Consulting

Learn how Halloran's assistance was able to improve a rare disease biotechnology company’s development and operations, communication workflow, and avoid the delay of a gene therapy trial.

DECENTRALIZED TRIALS

4 Ways Home Visits Support Successful Rare Disease Clinical Trials

Article | PCM Trials

Researchers, patients, pharma, and regulators face several obstacles when designing and conducting rare disease trials. Here, we delve into the importance of home visits in rare disease clinical trials.

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