08.15.25 -- Partners Ready To Support Your Phase 1-3 Trials

Revolutionize your approach to clinical trials at DPHARM: Disruptive Innovations to Modernize Clinical Research, taking place September 16–17, 2025, in Philadelphia. This conference showcases cutting-edge strategies and technologies designed to reduce patient and site burden, streamline operations, improve data quality, and accelerate access to therapies. Use code LSL20 for 20% off your registration.

What services are available to help you ensure continuous functional coverage, enhancing business continuity, operational efficiency, and risk mitigation?

With a focus on small and mid-sized biopharma companies, this premier CRO specializes in delivering innovative solutions in oncology and infectious diseases.

Whether you're aiming to run a pivotal trial or multiple studies, discover how Veristat's full-service support can drive your biologic therapies from inception to market success.

Choosing TFS means partnering with a CRO committed to clinical excellence and operational efficiency and advancing your ophthalmology study with precision and speed.

As a full-service CRO, Southern Star Research has the knowledge, industry relationships, and technical expertise to get your early-phase clinical trial up and running safely and efficiently.

Are you preparing to initiate your clinical trial? Trying to get your next milestone quickly? Determining whether to outsource? We can help you answer the questions that keep you up at night.

Novotech’s Regulatory Affairs team offers customized, end-to-end clinical and regulatory solutions, guiding biotech, pharma, and medical device companies through the entire product lifecycle.

Choosing the right CRO/CDMO for your first-in-human (FIH) trials enables you to run a successful study that generates high-quality data with speed and ease.

With over 30 years of experience, we provide comprehensive clinical pharmacology services, from data management and analysis to the generation of clinical study reports.

BRANY IRB provides pharma, biotech, and medical device companies with central IRB services that combine our service-first philosophy, our expertise and a proven, efficient process.

How can Ergomed use its oncology expertise, global reach, and access to patients with rare and ultra-rare diseases can help your organization achieve efficient, high-quality clinical trial execution?