Newsletter | March 13, 2025

03.13.25 -- Agile Functional Support To Accelerate Your Novel Therapies

Clinical Trials, Meet Adaptive Design

Traditional clinical trials can be lengthy and expensive. But what if there was a way to streamline the process, reduce costs, and potentially get life-saving treatments to patients faster? Enter adaptive designs – a game-changer in clinical research.

 

Global Regulatory Excellence Throughout The Clinical Development Lifecycle

Navigating the intricate global regulatory path is crucial for clinical development success. See how expert-backed support has consistently propelled sponsors toward regulatory excellence and embark on your own regulatory journey with our comprehensive suite of services.

 

Relieving The Strain Of Publishing During Regulatory Registration

Inherited data delays threatened a biopharma company's NDA submission for a new bipolar/schizophrenia treatment. Veristat, leveraging prior success, stepped in to streamline publishing and gain crucial FDA approval.

 

Enhance DMC Services By Harnessing Biostatistics Expertise

Discover how expert biostatistics and project management ensured data integrity and efficient DMC operations in a complex clinical trial for hematologic cancer cell therapies.

 

Medical Writing Support Relieves A Burdensome Review

A clinical-stage biopharmaceutical company dedicated to advancing innovative treatments sought out a crucial biostatistics and programming consultation. Discover how a medical writing and project management team was able to streamline the development and review of the company's critical marketing application document.

 

Strategic Clinical Consulting Success Stories

Explore real-world examples of how the combination of strategic consulting, regulatory insights, and technical expertise can impact the development and approval process.