We are delighted to see your interest in Freyr Webinar Series (FWS). The webinar on “IDMP is real; Redefine RIMS with the EMA’s SPOR operating model” is scheduled on December 02, 2021, for Americas, EUA & ROW regions.
What Is It All About?
IDMP has driven the redefinition of regulatory information management (RIM) systems to align with the emerging EU IDMP Implementation Guide (IG). This IG sets requirements for submission and management of data about medicinal products. Complying with the new EU target operating model (TOM) introduces new challenges for Sponsors, and we at Freyr can use our experiences to help you to conquer these challenges.
In the latest webinar from Freyr we are discussing the status of implementation of IDMP and SPOR in the European regulatory system and how you can confirm your readiness to comply with the emerging SPOR operating model.
Our expert with decades of experience will showcase the latest information about SPOR implementation and how we can prepare with our approach to ensuring high quality data and cost-benefits.
To help you understand the current practical considerations of the Swiss medical device industry, we bring you an exclusive live webinar on:
IDMP is real; Redefine RIMS with the EMA’s SPOR operating model
December 02, 2021
Duration – 45 Minutes
Join the Webinar at your Convenient Time
Director, Digital Automation
Simon joined Freyr to head digital transformation solutions in Europe, focusing on our flagship software solutions, including AiM and automation solutions. Before Freyr, Simon was with Oracle and had over 15 years of sales leadership experience working for IT companies supporting customers across the Life Sciences and Pharma sectors. In addition to working across Europe, Simon has lead bids in the US, Japan, and other global markets.
Senior Director for Regulatory Information Management Strategy
Gabriel brings a comprehensive experience of strategic delivery, business improvement, and operational transformation with 20+ years of professional experience gained working for different regulated industries. For the last 10 years Gabriel has specialized in regulatory operational improvement and health-related informatics and worked with both the European and UK medicines regulatory agencies
This webinar, ”IDMP is real; Redefine RIMS with the EMA’s SPOR operating model.” approaches for small and medium businesses, explains the following:
- IDMP and SPOR implementation – where are we now?
- The power of IDMP – what’s in it for me?
- Getting smart with IDMP – preparing for operational readiness
- Leading the race – the Freyr approach
- IDMP – What’s coming next from Freyr?
Given the keynotes and with due respect to your busy schedule, we look forward to seeing you in the webinar. Register now! Stay informed. Stay compliant.