Welcome To Trials Pro
Your trusted partner in clinical research and regulatory solutions
With a steadfast commitment to innovation and 30+ years of experience, we are your go-to Clinical Research Organization (CRO) for end-to-end solutions across various domains, including pharmaceuticals, biotech, medical devices, molecular and diagnostic clinical research, and regulatory compliance.
With our comprehensive suite of services, we provide end-to-end solutions that span from preclinical development to Phase IV trials in North America and worldwide, Clinical trials Management, CDM (Clinical Data Management), Regulatory filings, including ANDA, INDA, premarket approvals for Class I, Class II, and Class III medical devices, and post approval services.
Our Commitment to Excellence
Trials Pro is more than just a business; it’s a dedication to innovation in healthcare that goes above and beyond. We offer strategic insights and hands-on advice that streamline processes, find growth opportunities, and help you unlock your full revenue potential. We have been in this business for over 30 years and know a lot about it.
Why Choose Us?
Experience That Matters
Our seasoned team of experts has accumulated invaluable insights while collaborating with industry giants such as Abbott, Takeda, Pfizer, and many others. This experience empowers us to anticipate challenges, mitigate risks, and streamline the regulatory processes.
Innovation Driven
We thrive on staying at the forefront of clinical research and regulatory advancements. Our commitment to innovation ensures that you benefit from the latest methodologies and technologies, enabling faster, more cost-effective trials and approvals.
Patient Center Support
At Trials Pro, we put patients at the center of everything we do.Our research is designed to imporve patients lives and provide better treatment options for a wide range of medical conditions
Dedicated Support
We’re not just a service provider; we’re your partners in success. Our team works closely with you at every step, offering personalized guidance and support to ensure your projects meet or exceed their goals.
FAQ's
Trials Pro offers a comprehensive suite of services to support clinical research and regulatory needs. Our services include protocol development, regulatory strategy, patient recruitment, data management, statistical analysis, and regulatory submission support. We aim to streamline the entire research process, from concept to market approval.
Navigating regulatory compliance can be daunting, but Trials Pro is here to help. We provide expert guidance on meeting regulatory requirements, including FDA, EMA, and other global agencies. Our team can help you create a regulatory strategy, prepare and submit regulatory documents, and conduct compliance audits to ensure your project meets all necessary standards.
Trials Pro utilizes innovative approaches to patient recruitment and retention. We leverage data-driven strategies, and patient engagement techniques to ensure your trial reaches its enrollment goals. We understand the importance of retaining patients throughout the study, contributing to its success.
Absolutely! Trials Pro specializes in designing and managing complex clinical trials. Our experienced team can help you create robust study protocols, manage multi-site trials, implement adaptive designs, and oversee every aspect of your research project to ensure it’s executed efficiently and within budget.