Description:

This course provides an in-depth overview of the Identification of Medicinal Products (IDMP) standards which are crucial for the identification, tracking, and regulation of pharmaceutical and healthcare products. Participants will gain a comprehensive understanding of the various aspects of IDMP, including data models, terminologies, and regulatory requirements.

Key Highlights:

💡 Understand the IDMP in the pharmaceutical industry

💡 Learn about the IDMP Standards

💡 Understand the Benefits and Challenges in IDMP

💡 Explore the SPOR Data and IDMP Implementation Process

💡 Understand FDA approach on IDMP Standards

What you will learn:

✅ Deep Understanding of IDMP Standards
Learn the core concepts and principles of the IDMP standards and how they facilitate the identification and regulation of medicinal products.

✅ IDMP Benefits and Challenges to implementing IDMP
Explore the Benefits and Challenges used in IDMP and gain knowledge into how they can be implemented effectively.

✅  SPOR Data Management with IDMP
Familiarize yourself with the SPOR Data management used in IDMP and understand their role in ensuring accurate product identification and information exchange.

✅ Phases of Implemention of IDMP through SPOR Programme
Gain knowledge about the phases of IDMP Implementation through SPOR Programme and compliance guidelines related to IDMP and discover how to meet the requirements set by regulatory authorities.