Why Stryde?
Experienced PI's, SI's, CRCs, and Quality staff
They bring a wealth of knowledge and experience to the table, ensuring that the trial is conducted effectively and efficiently. Their expertise and attention to detail ensure that all regulations and protocols are followed, and that the study is of the highest quality, resulting in accurate and reliable results.
One budget, one contract, completed in less than three weeks
Streamlined and efficient process to eliminate the need for multiple budgets and contracts, reducing the administrative burden and saving time. The quick turnaround time ensures that you can move forward with your research plans sooner.
Expedited feasibility process
Efficient approach to evaluating the feasibility of a clinical trial, allows you to quickly determine if a trial is viable, reducing the time and resources required for the trial development process.
Central IRB (chosen by the sponsor)
Enable optimized review process, allowing for a more efficient and consistent evaluation of trials.
Comprehensive, standardized training for all team members
Team members are equipped with the knowledge and skills they need to deliver a high-quality trial
Quality source documents and data standardized in eSource and eReg
All data and documents in one centralized location makes it easier for trial sponsors to manage and monitor the study, reducing the risk of errors and improving efficiency.
A dedicated management team to oversee enrollment and quality
A single point of accountability for overseeing the trial, ensuring that all aspects are well managed and organized .