The training composed of 5 pre-recorded webinars, will enable you to effectively utilize IDMP-O and ensure regulatory compliance.
The IDMP-O training is designed to equip you with a comprehensive understanding of how the IDMP Ontology addresses complex challenges inherent in the IDMP domain. Delivered by the creators of the IDMP Ontology, this training will provide you with expert insights into the ontology’s structure, usage, and benefits, enabling you to effectively utilize it to streamline processes, enhance data interoperability, and ensure regulatory compliance within the pharmaceutical industry. Upon completing the course, participants can apply to join a one-year partnership program that includes accreditation to provide IDMP-O training consultancy.
Audience
• Pharma – general understanding. Roles: Data Managers, IT Managers, Leadership roles, IDMP-relevant data providers.
• Vendor companies – accreditation – pre-requisite for the partnership program.
• Standards Development Organizations
• Members of Pharma Trade Associations
Benefits
• IDMP-O implementation knowledge gain
• Certification for IDMP-O implementation
Agenda
Webinar 1: Introduction to IDMP
In the first webinar of our series, we introduce the IDMP standard and its importance, the relationship of the IDMP data model and standards to real live use cases (building upon those published by the Global IDMP Working Group) and relate this to both in-depth data definitions and practices as well as to application of the IDMP Ontology.
Webinar 2: IDMP-O overview and benefit
In this webinar we cover the benefits of IDMP implementation using IDMP-O, IDMP Data Elements and Standards addressed with IDMP-O, as well as Regulatory Compliance aspects.
Webinar 3: Getting started with IDMP-O
The webinar covers an introduction into the IDMP-O Project, the Methodology for the IDMP-O Development and insights into how to implement IDMP-O in your company.
Webinar 4: Use Cases
This session gives a general overview of methodology to build and implement IDMP-O based on pain points / use cases.
Webinar 5: IDMP-O Dependencies and Implementation Guide
The final webinar includes a Pharma Implementation Guide and IDMP-O Dependencies, as well as a presentation on how to expand global usage of IDMP standards for patient safety, incl. IDMP-O in PRISM, RWE and AI use cases.
Speakers
- Raphael Sergent, Accurids
- Asiyah Yu Lin, Pistoia Alliance
- Sheila Elz, Bayer
- Vada Perkins, PRISM
- Frits Stulp, Executive Board Member CTADHL, Life Sciences & Healthcare Industry Leader for the Netherlands at Deloitte
- Joerg Stueben, Boehringer Ingelheim
- Jeanneke Spruit, Senior Consultant Regulatory Information Management, Deloitte
- Max Fink, Boehringer-Ingelheim
- Prity Kumari, Boehringer-Ingelheim
- Norman Schmuff, FDA
- Aditya Tyagi, Pistoia Alliance
For questions or comments about the IDMP-O training, contact anca.ciobanu@pistoiaalliane.org
Prices
- Registration Fee (Pistoia Alliance members) $571 + booking fee
- Registration Fee (non-members) $1143 + booking fee