News

ENRICH USA -Financial Technology Webinar

ENRICH USA will invite you to the Financial Technology Webinar During this webinar, you will have the opportunity to learn more about the state of financial technology in the USA, along with cooperation with the EU. This webinar will be organized on Wednesday, August 5, 2020 at 16:30 CET / 10:30 Eastern Time. To register and consult the agenda, access the link https://register.gotowebinar.co...

MPP2020 Conference

The Medtech & Pharma Platform's annual conference is dedicated to products and solutions that combine medtech and pharma components. Why participate? Exchange of knowledge: Each year, prominent speakers from regulators, medical and pharmaceutical companies, government institutions, research laboratories, consulting firms and patient organizations share their ideas in this emerging fi...

Conference "Every day matters: improving time for patients' access to innovative cancer therapies in Europe

The EFPIA cancer platform invites you to participate in the virtual event "Every day counts" on September 21, 2020, which will mark the launch of "Every day counts: improving time for patients' access to innovative cancer therapies in Europe <https: //efpia-current.cmail19 com / t / iL-xkhtto-jtkydyjkur-j /> This publication presents the results of the "Patient Acces...

GCP training courses

The revision of the ICH-GCP Guide entered into force on 14 June 2017. It maintains the original text from 1996, but adds definitions, clarifications on the existing text and, in particular, adds a comprehensive section on risk-based quality management responsibilities of the sponsor. This training is intended for professionals working in clinical trials (investigators, clinical trial teams or r...

The European Commission has launched through the Funding & Tenders website the call "Shortening the path to Rare Disease diagnosis by using newborn genetic screening and digital technologies"

The European Commission has launched through the Funding & Tenders website the call "Shortening the path to Rare Disease diagnosis by using newborn genetic screening and digital technologies". The overall objective of this call topic is to shorten the path to RD diagnosis by using newborn / paediatric (infants during their first weeks of life) genetic screening; and, via application...