Skip navigation
Skip navigation
You are using an outdated browser. Please upgrade your browser.

The Webinar, “Taking a Strategic Approach to the Implementation of the IDMP,” to take place at 14:00 Central European Time on 18 September 2014

Cambridge, UK – September 15th, 2014 – Life sciences outsourcing and consulting services specialist ProductLife Group (PLG) has announced that the first event of its much-anticipated PLG Evolve autumn programme will focus on Identification of Medicinal Products (IDMP) compliance.

The Webinar, “Taking a Strategic Approach to the Implementation of the IDMP,” to take place at 14:00 Central European Time on 18 September 2014, will be led by life sciences industry heavyweights who will discuss the challenges pharmaceutical and medical device suppliers face as they prepare to comply with new requirements around medicinal product information submission in time for a European Union deadline of 1 July 2016. By that date, affected companies will have to meet the new IDMP global standards of the International Organization for Standardization.

With less than two years to go to get product data in order, consultant Andrew Marr, a renowned expert on the requirements stipulated by the latest product information standards, will copresent this timely session alongside Joerg Steuben, a Boehringer Ingelheim senior expert on quality and regulatory processes and documentation. The two will be joined by Sophie Daniel, head of quality, process, and information management at ProductLife Group.

Points of discussion will include:
• The scope of IDMP from both regulatory and broader health-care perspectives
• The steps involved in bringing IDMP to fruition, including the development of IDMP implementation guides
• Assessment and monitoring of regulatory developments in the lead-up to IDMP
• What IDMP means for companies and how to achieve an effective and compliant transition from the latest eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) standard to IDMP, its successor.

Originally designed to aid in identification of substances and medicines for pharmacovigilance purposes, IDMP has evolved into something much broader and deeper than its XEVMPD predecessor. There is also growing interest in using IDMP data for broader health-care purposes—for example, to support medical history provision for patients being treated in other countries.

In announcing the opening event, PLG chairman and CEO Pierre Cuny said, “We felt it was important to start our autumn schedule with a subject that will resonate with organisations right across our industry. Preparing for comprehensive product data compliance is no easy feat, especially now that the scope is so broad. Our speakers will be advocating a strategic, well-thought-out approach that creates maximum opportunity for companies to both satisfy regulatory requirements and deliver something beneficial for their businesses.”

To attend the Webinar, register here

Future events in the PLG Evolve programme—including additional Webinars, briefings, and breakfast meetings—will be announced soon.

About ProductLife Group

ProductLife Group is a trusted partner that helps clients stay ahead of the changing R&D landscape.
We provide support across all stages of the product life cycle and have experience in working with companies in all segments of the life sciences industry.

With an established presence in five European countries, extensive capabilities in key markets, and
more than two decades of serving the industry, ProductLife Group has a solid platform from which to provide clients a range of services, consulting, and outsourcing solutions. We empower clients to focus
on innovation and business growth strategies and to make strong, informed decisions every step of the way. What’s more, we wrap it all up with partnership flexibility, for a truly custom experience that helps clients scale their initiatives cost-effectively.

By leveraging the power of deep domain expertise, relationships, collaboration, and a flexible delivery framework, ProductLife Group delivers exceptional service to clients. Our goal is to develop long-term relationships by being responsive and relevant and by consistently delivering value. We cultivate a trusting, consultative environment and are positioned to operate as an extension of clients’ businesses, with a shared interest in their long-term success.

More at ProductLife Groupor follow us on Twitter at @ProductLife_EU.

Tags: ProductLife Group, PLG, life sciences, regulatory IM, reg IM, RIM, IDMP, pharmaceutical data management, Andrew Marr, Boehringer Ingelheim

PR Contact
Sarum PR – PR for ProductLife Group
+44 1722 322916
carina@sarumpr.com

This press release was distributed by ResponseSource Press Release Wire on behalf of Sarum PR in the following categories: Business & Finance, Medical & Pharmaceutical, Computing & Telecoms, for more information visit https://pressreleasewire.responsesource.com/about.