Safety, surveillance, post marketing studies

Safety and surveillance trials are a legal requirement throughout a drug’s lifetime, thus forming a crucial component of all post-marketing studies. The use of innovative mHealth approaches can support the comprehensive monitoring of drugs to ensure their ongoing safety and efficacy.

In addition, and driven by the increasing cost burden of healthcare, both clinical and cost effectiveness criteria have become vital measures for receiving market access or reimbursement for new drugs, devices and therapies. Vodafone mHealth Solutions can support patient retention and data capture in studies supporting health economics and outcomes research.

Case studies

Safety, surveillance, post marketing studies

Driven by the increasing cost burden of healthcare, both clinical as well as cost effectiveness criteria have become vital measures for receiving market access or reimbursement of new drugs, devices and therapies. Vodafone supported a big pharmaceutical customer with a resource utilisation study amongst 300 epileptic patients across three countries.

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