Self-Care
Novel Food webinar Preview
Webinar about Novel Food regulatory Framework and scientific requirements for novel Foods - Preview
Pharmacovigilance
Key considerations when building a global PV program
earn more about the key considerations when establishing a global PV program, focusing on the essential role of LSO and LPPV
Medtech
๐ฃ๐ฟ๐ผ๐ฎ๐ฐ๐๐ถ๐๐ฒ ๐ฎ๐ป๐ฑ ๐ฅ๐ฒ๐ฎ๐ฐ๐๐ถ๐๐ฒ ๐ฃ๐ผ๐๐-๐ ๐ฎ๐ฟ๐ธ๐ฒ๐ ๐ฆ๐๐ฟ๐๐ฒ๐ถ๐น๐น๐ฎ๐ป๐ฐ๐ฒ: ๐๐บ๐ฝ๐น๐ฒ๐บ๐ฒ๐ป๐๐ฎ๐๐ถ๐ผ๐ป ๐ง๐ถ๐ฝ๐
Are you looking to optimize your Post-Market Surveillance (PMS) process and stay compliant with the latest regulatory requirements? Watch out our webinar!
Innovation
Product Develoment
CTIS โ Insights of the new system’s challenges
We guide you through the key features of the Clinical Trial Information System (CTIS) to help you successfully submit your trial applications and manage the transition process.
Regulatory affairs
Relations avec les Organismes Notifiรฉs
Dans le cadre de la mise en ลuvre du Rรจglement (UE) 2017/745, les relations entre les organismes notifiรฉs et les fabricants de dispositifs mรฉdicaux peuvent devenir plus complexes, ce qui peut affecter vos dรฉmarches
Product Develoment
Prime Scheme – A Tailored Development
Medtech
Clinical Validation of Software Integrating AI
Pharmacovigilance
Integrating Local PV System into Global PV System
Quality compliance