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Pharmacovigilance & Patient Safety - Medsafbiopharma

My Desk

Postmarketing surveillance is monitoring the safety of a pharmaceutical drug or medical device after it has been released on the market and is an important part of the science of pharmacovigilance.

Brooklyn Design

Our skilful global team tailor-make solutions for any clinical and post-marketing pharmacovigilance (PV) obligations, compliant with EMA, FDA and ICH. We ensure that this is a comprehensive yet cost-effective process, enabling full compliance with legal requirements. We have a team of fully qualified medical professionals acting as QPPV’s with European, US or Global coverage.

We provide a comprehensive range of drug safety services to help minimize risk and protect patient well-being.

Way of Life

Clinical trial participants help us speed breakthroughs in modern drug development. Our job is to protect them. From versatile technologies and targeted data collection and analysis to in-depth reporting and regulatory compliance, we provide a comprehensive range of pharmacovigilance services throughout the product life cycle to detect, assess, understand, and prevent adverse effects or any other drug-related issues, ultimately making patients’ lives better.

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