11.17.23 -- Partners Ready To Support Your Phase I-III Trials

As one of the world’s largest and most experienced safety and PV organizations, unearth how this provider is bringing extensive expertise and regulatory intelligence to every industry engagement.

Get the assistance your teams need to translate exceptional concepts and groundbreaking science into transformative treatments that bring hope to those facing unmet medical needs.

Altasciences is an award-winning, forward-thinking, mid-size early phase contract research organization, in Canada and the U.S., offering biopharmaceutical companies of all sizes a proven, flexible approach to early drug development.

Inspired by excellence and empowered by people, explore how inSeption Group is able to work as a full-service outsourcing solution to meet and exceed study expectations.

IQVIA Biotech is a standalone business of IQVIA with dedicated teams delivering clinical development solutions for biotech and emerging biopharma customers. Discover why IQVIA Biotech is the CRO partner of choice for biotech companies around the world.

Novotech has built teams with deep expertise in oncology and immuno-oncology and strong connections with oncology key opinion leaders and sites in the Asia-Pacific region.

Biorasi provides the swiftness and flexibility required by contemporary small and midsize pharmaceutical and medical device firms. Our unique approach to clinical research expedites the completion of clinical trials, ensuring rapid results.

OCT Oncology™ is a comprehensive solution designed to support pharmaceutical companies throughout the entire lifecycle of oncology treatment development. OCT Clinical boasts a network of 300 top-tier oncology clinics spanning 10 countries.

Whether it's for a single study or multiple studies spanning various programs, Harbor Clinical's subject matter experts will diligently oversee the cleansing, management, and visualization of your data.

Veristat has assembled an extraordinary team of scientific-minded experts who strategically design and execute clinical trials and prepare your clinical data for regulatory review.