As a leading Contract Research Organization (CRO) with over 40 years’ experience, we are uniquely placed to help you design, develop and implement clinical trial solutions for your projects. We help optimize your timelines cost-efficiently to bring your product to market quickly and safely. We support you with fast testing and development processes, enabling you to make safe ‘go/no go’ decisions about your product that are based on the most reliable data. As the leading biometrics CRO with a state-of-the-art Clinical Pharmacology Unit, we have the resources and expertise to support you at every step.
As a full service CRO, we offer:
- Strategic input and consulting
- Regulatory support
- Clinical trial management and monitoring
- Data management and Electronic Data Capture (EDC)
- Biostatistics and statistical programming
- Medical writing
- Medical safety
- Data and Safety Monitoring Board (DSMB) and clinical events committees
- Clinical trial laboratory testing
We cover multiple therapeutic areas with a focus on infectious diseases, respiratory, oncology and dermatology.
To discuss your clinical research outsourcing requirements, contact us today.
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