Clinical Trial Study Start-Up
Accelerating Clinical Trial Initiations with Customized Study Start-Up Solutions
Altasciences provides comprehensive clinical research services and solutions. Our specialized teams collaborate to provide you with strategic insight and safely expedite study start-ups whether you work with one or more of our clinical sites as well as with a partner site. We are strategically located across North America and have in-depth experience working with sponsors worldwide. We expertly navigate complex regulatory landscapes, engage with ethics committees, and manage site contracts and budgets, so you don’t have to.
Clinical Trial Study Start-Up Strategy for Successful Initiation
Our project team efficiently manages your clinical trial start-up. They define planning elements as early as possible, ensure rapid completion of reviews, and obtain necessary clearances from governmental bodies. Our streamlined approach guarantees that your clinical activities start on time.
- Tailored Strategy: We combine strategic planning, deep knowledge, and a tailored approach to prepare for potential regulatory hurdles and align with your study's unique needs. This involves essential documents, contract reviews, and individualized strategies for site initiation.
- Knowledge: Our start-up teams have a proven track record of commencing clinical trials across North America, offering a rich blend of diverse clinical operations expertise and extensive industry experience.
- Communication: Leveraging centralized program management and proprietary communication platforms, we ensure comprehensive and efficient discussions about all necessary study start-up requirements. Our proprietary scheduling platform streamlines interactions, minimizes downtime, and expedites the clinical trial start-up process. Our commitment to effective communication is pivotal in eliminating inefficiencies and accelerating trial start-up.
Managing Site Activations
Because we believe familiarity and continuity make for a more enjoyable and smooth clinical trial start-up experience, we will assign you a designated project manager (PM) and a dedicated team of specialists for the lifecycle of your study. Together, they determine the optimal start-up timelines for each clinical site required, and ensure we stay on track. This ensures consistency and smooth transitions, such as for amendments or adding new sites.
Want to learn more about our process for identifying, selecting, and managing clinical trials? Explore further on our website by visiting the following pages: