Complex early phase trial? We can help.
As you plan for future development, our team can support both your bioanalysis and clinical pharmacology needs. It is our mission to deliver better data, faster, without compromising quality, allowing your asset to accelerate to the next step.
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Worldwide is your clinical and bioanalytical one stop shop.
Our bioanalytical lab and Clinical Pharmacology Unit are within one-hour driving distance from each other, offering a comprehensive approach that benefits our clients through streamlined vendor management, consistent standards and overall efficiencies in project management that ensure quality and save you time and money.
State-of-the-art Bioanalytical Facility
- 60,000 sq. ft. laboratory building located in Austin, TX, with excellent audit record
- Capacity to accommodate your bioanalysis needs immediately
- Capabilities in small molecule and biologics, including PK, immunogenicity, and biomarkers
- Long history of bioanalytical experience in developing and validating bioanalytical assays in support of GLP and clinical studies
- Collaborative network of teams including large molecule assay development, small molecule assay development, assay validation, sample testing, automation, BSM, sample management, and quality
- End-to-end bioanalytical service as our lab assists with critical reagents generation, labeling, and characterization, TK/PK data analysis, and report preparation
Clinical Pharmacology Unit
- 200-bed, highly flexible, fit-for-purpose unit in San Antonio, TX, with access to over 2.5 million subjects within the San Antonio metropolitan area
- Conducts trials in healthy volunteers, patients, and specialty populations including, overweight/obese, post-menopausal/surgically sterile females, healthy elderly, renal impairment, hepatic impairment, metabolic syndrome, T2DM, dyslipidemias, and NASH
- 17-year track record across a wide range of ClinPharm Studies from design to report
- Ability to offer full-service early and late stage development study conduct under one set of SOPs
- Fully validated eSource data collection system
- cGMP Phase I Pharmacy and CLIA Safety Lab onsite
“During the bid defense, I felt like, at the highest level, that Worldwide was really trying to develop a relationship with us and work with us. And I think that, though it may be a splitting hairs sort of differentiation, we view our CRO as an extension of our team, not a subsidiary of our team."
When battling tight timelines, keep your program accelerating to approval by choosing Worldwide Clinical Trials.
