The training composed of 5 webinars, 90 minutes each, 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
The webinars will run at the dates mentioned below and will include live Q&A sessions.
Participants who are unable to join the live sessions due to business priorities or time zone differences can request on-demand access.
Webinar 1: Introduction to IDMP
November 19, 2024
In the first webinar of our series, we’ll 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.
Speakers
- Frits Stulp, Executive Board Member CTADHL, Life Sciences & Healthcare Industry Leader for the Netherlands at Deloitte
- Jeanneke Spruit, Senior Consultant Regulatory Information Management, Deloitte
Webinar 2: IDMP-O overview and benefits
November 25, 2024
In this webinar we will cover the benefits of IDMP implementation using IDMP-O, IDMP Data Elements and Standards addressed with IDMP-O, as well as Regulatory Compliance aspects.
Speakers
- Sheila Elz, Bayer
- Joerg Stueben, Boehringer Ingelheim
Webinar 3: Getting started with IDMP-O
December 5, 2024
The webinar will cover 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.
Speakers
- Aditya Tyagi, Pistoia Alliance
- Max Fink, Boehringer-Ingelheim
Webinar 4: Use Cases
December 10, 2024
The webinar will cover a general overview of methodology to build and implement IDMP-O based on pain points / use cases.
Speakers
- Raphael Sergent, Accurids
- Max Fink, Boehringer-Ingelheim
- Prity Kumari, Boehringer-Ingelheim
- Norman Schmuff, FDA
Webinar 5: IDMP-O Dependencies and Implementation Guide
December 12, 2024
The webinar will include a Pharma Implementation Guide and IDMP-O Dependencies, as well as a presentation on how to expand 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
For questions or comments about the IDMP-O training, contact anca.ciobanu@pistoiaalliane.org
The schedule and speakers are subject to change. The webinars are recorded and can be accessed on-demand
Prices
- 30% Discount by 31 October 2024 (members) $400 + booking fee
- 30% Discount by 31 October2024 (non-members) $800 + booking fee
- Registration Fee (Pistoia Alliance members) $571 + booking fee
- Registration Fee (non-members) $1143 + booking fee