Our Life science webinars

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

𝗣𝗿𝗼𝗮𝗰𝘁𝗶𝘃𝗲 𝗮𝗻𝗱 𝗥𝗲𝗮𝗰𝘁𝗶𝘃𝗲 𝗣𝗼𝘀𝘁-𝗠𝗮𝗿𝗸𝗲𝘁 𝗦𝘂𝗿𝘃𝗲𝗶𝗹𝗹𝗮𝗻𝗰𝗲: 𝗜𝗺𝗽𝗹𝗲𝗺𝗲𝗻𝘁𝗮𝘁𝗶𝗼𝗻 𝗧𝗶𝗽𝘀

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 – 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.

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

Annex 1 Changes and challenges: a concrete return of experience from the clients

Product Develoment

Acceptance of NDA/MAA with only Chinese Patients by Western Regulatory Agency

Innovation

Regulatory Operations

How to use regulatory document sources to build an IDMP data model?