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SCOPE’s drug safety physicians, who have many years of both clinical and research experience, will ensure that your trial progresses safely. We perform proactive and ongoing activities that aim to minimize harm and maximize the benefit of products during their development, ensuring patient safety and public health. By working closely with your study team and by combining our medical monitoring services with data management, we are able to continuously provide you with high-quality safety feedback. We supply a complete range of medical services – medical monitoring, medical writing, medical coding, pharmacovigilance and 24/7 consulting. With our extensive medical know-how and experience, we also offer scientific advice to support your trial.
Always vigilant with your product safety
SCOPE provides full drug safety services for your study – from serious adverse event management to data reconciliation and study closure related activities. Our experts proceed with case handling and safety submissions to all regulatory authorities and ethics committees according to local requirements and international standards.
Physician-led medical monitoring
With our extensive medical experience, we can help to resolve all trial-related medical issues. From setting up medical protocols and providing team training to offering 24/7 medical support and data review, SCOPE covers all your medical monitoring requirements and more. Our proactive approach enables us to identify potential issues and prepare accordingly, thereby reducing risks, timelines and costs.
