Our Approach to Successful Clinical Development
Working Together to Solve Complex Challenges and Deliver Results.
What makes for a positive client experience? At Veristat, we believe it is based on our ability to accomplish more, more effectively and with less worry for you. With flexible and scalable engagement models and unparalleled expertise, we support your success by orchestrating and conducting activities that accelerate access to high-quality therapies globally.
Customized Engagement Models to Support Success
Veristat has been a trusted source of intellectual leadership and scientific-minded guidance in clinical development to guide your critical decision-making. We provide strategic level thinking to help clients optimize their clinical development approaches, program planning/trial designs and regulatory submission strategies. Learn More
We can project manage every aspect of your trial or just provide supplemental services to round out your team. Our experts collaborate with you by providing strategic consultation throughout your program, clinical operations support, safety management, data management, CDISC implementation, biostatistics, statistical programming, medical writing and regulatory submissions support. Learn More
Our project managers, medical writers, data managers, data standards team, biostatisticians, statistical programmers, and regulatory affairs experts work tirelessly in unison to successfully prepare regulatory strategies and marketing applications. As testament, our teams have prepared over 160 regulatory marketing applications that have led to more than 80 regulatory approvals to date. We executed a flawless regulatory submission process which helped lead to their approval. Learn More