IDMP Consulting_

Improving patient safety across the world with next-generation data standards.

Identification of Medicinal Products (IDMP) is a suite of five standards developed within the International Organisation for Standardisation to facilitate the unique identification of medicinal products in the context of pharmacovigilance and the safety of medications throughout the world.

This new set of data standards will revolutionise the manufacturing, distribution, and regulation of medicinal products globally. It establishes data standardisation throughout the entire product lifecycle, encompassing development, investigational products, evaluation, and authorised products.

IDMP aims to enhance the reliable exchange of medicinal product information, promoting interoperability across regulatory and healthcare communities worldwide. This fosters accurate analysis and unambiguous communication across jurisdictions.

Our consultancy services are specifically tailored to assist organisations in successfully implementing and complying with the Identification of Medicinal Products (IDMP) standards.

Our team of experts possess a deep understanding of the intricacies of healthcare regulations and the criticality of standardised data and structures for medicinal products. Leveraging our expertise, we offer comprehensive solutions to guide you through the IDMP implementation journey, enabling you to achieve optimal results and stay ahead of regulatory requirements.

Our Approach

We Can Help With_

IDMP Readiness Assessment

Conduct a thorough analysis of your current systems, processes, and data to assess your readiness for IDMP compliance. Our experts identify any gaps or areas that require improvement and provide you with a detailed roadmap.

IDMP Strategy and Planning

Develop a customised IDMP strategy and implementation plan aligned with your organisation’s goals and resources. Our consultants work closely with you to ensure a seamless integration of IDMP standards into your existing systems and processes.

Technical Implementation Support

Assistance in the technical implementation of the five ISO IDMP standards. We provide guidance on data architecture, data mapping, system integration, and data quality assurance, ensuring accurate and standardised product information across your organisation.

Data Management and Governance

Establish robust data management practices and governance frameworks to ensure ongoing compliance with IDMP standards. Our consultants assist in designing data models, data dictionaries, and data maintenance processes to enable efficient data exchange and reporting.

Training and Change Management

Tailored training programs to equip your employees with the necessary knowledge and skills to effectively navigate the IDMP landscape. Additionally, we provide change management support to facilitate a smooth transition and foster organisational alignment.

How IDMP is Transforming Healthcare

Pharmacovigilance: IDMP will improve the signal detection and response efforts to adverse event reports, as it looks to ensure harmonised product definitions, improve data quality for signal management and expedite communication, decision-making, and regulatory actions. Streamlining the Identification and management of adverse reactions will enhance patient safety across the globe.

Regulatory submissions: IDMP ensures consistent data standards enable the accurate capturing and management of information, facilitating sharing and reuse of medicinal product data across procedures and regulators. Meeting IDMP standards will decrease time to market for vital medicines.

Clinical trials: Agreed upon and well-supported standards grant stakeholders access to clinical trial data, delivering more control and improving assessments, scientific evaluation of medicines, and fostering communication and transparency. Clinical trials will become safer and more accurate resulting in improved patient outcomes.

Good manufacturing practice: Inspections of manufacturing sites utilise accessible information on how the products are manufactured, including ingredients and quantities. IDMP will streamline inspections, particularly for urgent situations involving defects. Consistent data standards also aid in the prompt detection of falsified medicines.

Why CloudKubed?

Data Experts

We have a highly skilled team of data consultants, architects, modellers, scientists and analysts who understand the nuances of data compliance and regulations. We help you to develop your own sustainable data capability by introducing data governance and up-skilling your internal teams.

Committed to Researcher Needs

Working with the UK’s Medicines and Healthcare regulator, we have been leading the UK’s first healthcare implementation of IDMP standards. Our experts have a deep understanding of IDMP standards and how they should be implemented across industries.

Cloud & ResearchOps excellence

We have led and delivered digital and data transformation programmes for large UK Public Sector healthcare agencies. Our team also has extensive experience in the pharmaceutical sector, we understand the problems that inconsistent data standards poses to improving patient care and interoperability within these industries.