Iperion is the leading expert on IDMP implementation
Iperion is at the center of the discussions with both Industry and Regulators
Iperion is directly involved in:
- the ISO IDMP discussion
- review of the EU Implementation Guide (IG)
- setup EU-Substance Registration System (EU-SRS)
- leading IRISS forum
We have a proven track record with our clients for IDMP consultancy
Our approach to IDMP implementation
- Awareness creation
Iperion experts provide customized sessions which establish appropriate understanding on IDMP, its impact and benefits for all levels within your organization
- Maturity Assessment
Together with you, we analyze your data, processes, organization and technology to define your future IDMP needs
- Planning & Setup
We deliver a strategic vision for IDMP, based on best practices and fitting your unique business environment. Accordingly, we establish a pragmatic roadmap to implement your ideal solution
- Solution Implementation
We support the implementation of the desired solution, while making sure that all stakeholders are appropriately engaged, and objectives are achieved
We make sure that you have the correct and complete data for both development and registered medicinal products, comply with the internal and regulator needs. We can additionally strengthen and stabilize your maintenance operations by providing trained experts. Learn more about our managed services.
What is IDMP ?
IDentification of Medicinal Products (IDMP) is a data model, described in a set of five ISO standards and is used to describe the product and its characteristics.
- provides structured medicinal, pharmaceutical product and substance data models
- provides mechanisms to uniquely identify products and its components
- is the only global standard for medicinal product information
- is applicable to industry and regulators (in similar fashion as ISO 9001; Quality Management and other ISO standards)
IDMP is a global standard accepted by all 163 ISO member countries
Across the board industry stakeholders and health authorities are implementing IDMP. In the European Union this implementation is in the form of SPOR, Master Data Management product on Substances, Products, Organizations and Referentials.
SPOR data is meant to optimize the use of data across different processes (regulatory, pharmacovigilance, clinical, production, etc.) and IT tools (eAF, IRIS portal, CESP, CTA, EMVS, etc.).
What is the impact of IDMP implementation for your organization?
IDMP will change the way of communication with the regulators.
Together with the current document-based submission, structured medicinal product data will be submitted, reviewed and approved during the regulatory activity.
To meet this change in requirement, your company will need to transition towards a data-driven organization, which can optimize internal processes and sharing of information between different technology solutions and departments.
Based on experience, we know that this transformation takes time, as it requires buy-in from multiple stakeholders, adaptation of processes and technological landscape. Therefore, it is paramount to start now!
With our experience in IDMP implementation strategies, regulatory operations combined with extensive production experience, we can support you in making sure that this transformation goes smoothly.
How IDMP-ready are you?
With the mandatory use of PMS approaching it is time to take the necessary steps to smoothen the transition towards IDMP implementation. But how IDMP-ready are you? To find out your current state compared to the desired state before implementing IDMP, we have designed a questionnaire.
After submission you will receive a personal report including a presentation on your results by one of our IDMP specialist on your next steps and topics that require your attention from an IDMP readiness point of view. You will receive this report without any obligation.Find out how IDMP-ready you are by taking our questionnaire