Critical development milestones delivered with ease
Meeting drug interaction and other clinical pharmacology study timelines to complete your full NDA package while working on your pivotal Phase III study is a challenging requirement. Worldwide has the experience, the expertise, and the proven ability to take on all your clinical pharmacology studies so that you can move on to your next critical milestone.
Full Suite of Clinical Pharmacology Studies
First-in-Human
Integrated SAD and MAD (includes FE / DDI / BA / EPQT)
Drug-Drug Interaction
BE / BA
Food and Meal Timing Effect
PK / PD
AME / Mass Balance / Metabolite Profiling
Renal Impairment
Hepatic Impairment
Expert Precision QT and Thorough QT Evaluations Impairment
POC Studies in Patients
CSF Collection and Analysis
Specialty Procedures (Biopsies, NG tube, and unique routes of administration)
As you plan for future development, our team at Worldwide is here to support you.
Streamlined communication with a single study management point of contact for all clinical pharmacology studies
Immediate access to senior leadership for consultation and escalations
Expert advice on study design, including protocol and analysis plan development to accommodate conventional and nonconventional products
Fit-for-purpose facility co-located with our bioanalytical lab for efficient timelines and streamlined processes
Are you searching for a new partner to manage your bioanalytical needs? From method development or transfer to sample analysis and data generation, our state-of-the-art bioanalytical lab is fully prepared to assist, helping you streamline your outsourcing process. The benefits are clear: our co-located Phase 1 unit and bioanalytical lab translate to operational and communication efficiencies for you.
Our industry thought leaders and seasoned professionals are ready to consult and advise your next project to optimize data and give you the competitive advantage you deserve. Meet a few of our team members.
Executive Vice President and General Manager, Early Phase
Hear from our past customers about their experience with Worldwide
“During the RFP process, Worldwide Clinical Trials was highly responsive, and their medical and scientific expertise in understanding the clinical trial was something from our end that was truly outstanding compared to other CROs that responded to us.”
“The proposal that Worldwide Clinical Trials gave us was the most insightful in terms of suggesting some specifics strategies that the others CROs didn’t include.”
“They have the expertise in-house. They really blew it out of the park – during the bid defense, the ad hoc questions, and even in the one-hour session where they solidified their position as to why we should work with them. But I have to say that the major factor was the internal expertise. It was just terrific the amount of knowledge the team had in the indication and the connections they had.”
Study consultation, execution, and quality data – delivered with the highest level of service and transparency.
Schedule a consultation with our team
We use cookies to ensure our website functions properly and to enhance your experience. See our Cookie Policy for details. Select your preference to continue.