EU IVDR – Clinical Evidence and Performance Evaluation by Andrea Colombo, MD Compliance Expert – PQE Group The issues exposed in this article will be discussed in “In Vitro Diagnostic Medical Device Regulation 746/2017: what to know to be ready” free Webinar by PQE, on July 8th @11:30 a.m. CET – Register now to secure […]
The European Council and Parliament officially adopted an amendment to Regulation 2017/745, modifying the most of application dates to May 2021.
Why MD Cybersecurity is so important by Danilo Maruccia, Executive Consultant & Business Partner – PQE Group Is Cybersecurity important for Medical Devices? The answer is absolutely yes. But let’s move a bit backwards, to understand the reason why nowadays Cybersecurity has become a main concern for all Medical Devices producers.
Pharmaceutical and MD companies now have a brand new channel for their inbound marketing activities on the Italian market. In fact, after the new Advertising Guidelines issued by Italian Ministry of Health, Facebook decided to open their platform to Pharma OTC and OTC-MD adv campaigns: a huge B2C market is about to be at reach […]
Madrid (Spain) – October 9th -11th, 2018
Tokyo (Japan) ● March 18th – 20th, 2019
Bruxelles (Belgium) ● June 17th – 21st, 2019.