Bluereg > ICSR Management – Case processing
BlueReg can offer you a complete service for adverse event case processing during clinical trials and post-authorisation; from collection and medical assessment right through to submission to the health authorities. We have the flexibility of using your own database or our own fully validated database. At BlueReg we understand the importance of case processing and ensuring a high-quality service is provided in accordance with global requirements from start to finish. Our consultants always follow current international guidance and ensure agency reporting requirements are met. For a full breakdown of all the services we offer in relation case management please get in touch with us. We can tailor the services to provide you with the perfect package.