Industry Specific Services: ISO IDMP
IDMP compliance is an opportunity for more efficient processes - with msg industry advisors, you can achieve an efficient, legally compliant and holistic implementation that meets the EU regulation regarding the ISO IDMP data standard.
New EU regulation (IDMP - Identification of Medicinal Products) sets high expectations for the exchange of product information
New EU regulation (IDMP - Identification of Medicinal Products) sets high expectations for the exchange of product information The EU regulation on the identification of medicinal products (IDMP) introduces new requirements for the exchange of product information between manufacturers, regulatory authorities, suppliers and distributors. In future, pharmaceutical and biotech companies are obliged to transmit and maintain detailed product information in electronic form at all times. This presents a major challenge for manufacturers and requires considerable changes to existing product-related processes and systems.
msg industry advisors will accompany you through this challenging transformation and support you in all phases of your IDMP implementation project.
IDMP implementation as an opportunity for more efficient processes
As part of IDMP implementation, pharma and biotech companies need to overcome traditional interdepartmental barriers and implement robust guidelines to ensure data governance. When implemented correctly, IDMP offers pharma and biotech companies the opportunity to sustainably optimize their business and regulatory processes by standardizing drug data and creating a “single source of truth” of information within the company.
However, this requires a holistic approach that not only considers technological aspects but also the organization and its processes. It is necessary to adapt the roles and responsibilities in the Regulatory Affairs unit as well as its cross-functional cooperation with other specialist departments. Another aspect is ensuring data quality and availability throughout the entire life cycle and implementing IT systems to enable the IDMP-compliant, automated transfer of product data to the EMA and, in future, to other agencies such as the FDA.
Our holistic approach for your IDMP transformation
msg industry advisors offer you a comprehensive portfolio of services to improve your IDMP capability depending on your needs and your current progress. We take a holistic IDMP approach that covers the areas of processes, organization, data and technologies to ensure full compliance with the requirements.
Our services include:
Awareness & communication:
Maturity level assessment:
We analyze data quality and availability, processes and your existing IT landscape to obtain a comprehensive picture of your IDMP maturity level.
Roadmap & setup:
Implementation:
Support:
Are you looking for ways to make your organization IDMP-ready?
We have the right approach for each phase of the IDMP implementation.
Further expertise on data management & analytics
Data & Analytics Strategy
Implement a well thought-out data & analytics strategy for high-quality and usable data.
Data Architecture
Increase not only your data quality, but also the information value of your data thanks to an optimized and integrated data infrastructure.
Master Data Management
With sustainable master data management, we create the basis for the highest master data quality – and thus guarantee industry standards.