Webinar – Materiovigilance – All you need to know about the new European regulation on Medical Devices (RUE 2017/745)
Universal Medica pleased to announce its next webinar on Friday 23rd of October 2020. Our experts will present the new European regulation on post-marketing surveillance of medical devices and will discuss the following points: – How to set up post-marketing surveillance of MDs and what data to monitor? – How is incident reporting carried out? – What are the periodic reports to be written, for…
7 key points for a successful pharmacovigilance inspection
On 18/06/2020 at 17h30 (30 minutes).
Pharmacovigilance is one of the cornerstones of a drug’s life. On a daily basis, it enables the monitoring and prevention of the risk of adverse effects resulting from their use. The announcement of a pharmacovigilance inspection is an important step in the life of a pharmaceutical laboratory…
5 key steps to manage crisis management in the pharmaceutical industry*
On 25/06/2020 at 17H30 (30 minutes)
Pharmaceutical companies are confronted with crisis situations that can have major consequences in terms of image, reputation and relationships with their direct or indirect customers. Whatever the type of crisis to be managed (shortage, industrial accident, unexpected adverse reaction, health crisis…)