Correct study choice and effective execution are paramount to achieving the desired goals
Peri-Approval and Observational studies are used to generate real world evidence, address questions pertaining to disease states and treatment patterns, provide early access to therapies, address questions pertaining to safety surveillance, risk management and efficacy.
ICON Commercialisation & Outcomes is experienced in the design and implementation of these studies to collect real-world data with a focus on maximising the return on investment. These include:
- Disease, Product Registries and Exposure Registries
- Global Phase IIIB and IV Clinical Trials
- Expanded Access, Named Patient Programs and Compassionate Use
- Non-interventional, Observational Research
Our experts also provide Safety Surveillance and Risk Evaluation Mitigation Strategies (REMS) to help you develop the best strategies that minimise risk and maximise benefit at the outset.