Worldwide Clinical Trials

Worldwide Clinical Trials is a global CRO providing full-service drug development services to the pharmaceutical and biotechnology industries across the full continuum – from early-phase and bioanalytical sciences through Phase II and III trials to peri- approval studies.
At Worldwide Clinical Trials we believe successful drug development is built upon a foundation which strategically balances science, medicine, operations and commercial intelligence. Our highly consultative approach around the needs of our clients ensures that we approach every Phase I-IV drug development program as unique. Our mission is to foster the development of life changing medicines by
integrating innovative methodology, rigorous science and efficient technology.
The extensive medical and scientific heritage of our team combines to offer WCT clients a wealth of expertise in CNS, cardiovascular, oncology, chronic inflammatory diseases as well as many additional therapeutic areas. Our deep experience drives the knowledge, methodological rigour and expertise in linking experimental design with operational imperatives needed for the successful completion of global clinical trials.
Combining our widely recognised therapeutic expertise with a robust global operations platform, we successfully manage clinical trials with our own staff across nearly 60 countries in North America, Latin America, Europe, Asia Pacific and the Middle East.
Our full-service capabilities enable us to meet particular trial requirements without compromising on science, safety or service.

Bioanalytical/immunoassay
• Biomarker development
• Method transfer and validation
• Pharmacokinetic analysis and reporting

Clinical research services
• Clinical pharmacology
• Bridging studies
• Dyna-bridging studies
• Drug-drug interactions
• Pharmacodynamic modelling

Clinical development
• Protocol development
• Feasibility
• Project management
• Medical monitoring
• Clinical monitoring
• Site management
• Data management
• Rater training
• Biostatistics and data analysis
• Medical writing
• Regulatory affairs
• Quality assurance
• Drug and supply depots
• Drug safety

Peri-approval
• Product safety and pharmacovigilance
• Late-stage research
• Registries and observational studies
• Health outcomes, epidemiology and risk management