WORLDWIDE CLINICAL TRIALS: AN UNCOMMON EARLY PHASE CRO
In the critical early study phases of your novel drug, you are hyper focused on proving the viability of your concept and ensuring the safety of your patients. But beyond that, you are laying the groundwork for the advanced phases of study that are yet to come. To get your compound off on the right foot, the design of your early phase trial must be rigorously strategic, and the protocol execution must be meticulous. When choosing Worldwide Clinical Trials as your early phase CRO, you will experience firsthand why we call ourselves the Cure for the Common CRO. We are confident that you will experience top-quality data collected under state-of-the-art laboratory conditions designed to put safety first while also making the best use of your financial investment.
A FULL-SERVICE EARLY PHASE CRO
We offer a range of early phase contract research organization (CRO) services executed by professionals fully dedicated to your early development program.
These services include:
- Protocol design and early phase concept and program development
- Protocol writing
- Regulatory and pre-IND/IND meeting consultation services
- Scientific consultation
- Multi-site feasibility support based upon established QA-approved site network
- Dedicated Phase I/early development project management group
- Phase 1 focused data management
- Biostatistics and statistical design planning specific to early development studies
- Pharmacokinetics
- Clinical monitoring
- Pharmacovigilance
- Site management
- Medical writing
INVESTING IN PATIENTS
Because patient care and data quality are our top priorities, we invest heavily in our subject recruitment efforts. Using both traditional and novel approaches, we have access to the healthy volunteers and specialized patient groups that you seek. Ready to see how specialized we can get? Learn more about the groups we have access to that you’ll be hard-pressed to find elsewhere.