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New Qualified Person Oversight Regulations When Importing Investigational Medicinal Product to the UK, Upcoming Webinar Hosted by Xtalks

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As of January 1st, 2022, IMPs imported into Great Britain from approved countries (EU) will require a UK Manufacturing and Import Authorisation (MIA(IMP)) holder to have in place an assurance system to check that these IMPs have been certified by QP before release to the trial.


TORONTO (PRWEB)

Qualified Person (QP) Oversight — Know how the new rules for importing finished investigational medicinal products (IMPs) into Great Britain from approved countries affects a clinical trial supply? As of January 1st, 2022, IMPs imported into Great Britain from approved countries (EU) will require a UK Manufacturing and Import Authorisation (MIA(IMP)) holder to have in place an assurance system to check that these IMPs have been certified by QP before release to the trial.

This webinar will describe:


  •     The importation routes available — direct to site or through a UK Distribution Hub

  •     The authorisations required by the UK MIA(IMP) holder and the clinical trial sponsor

  •     The assurance system required of the UK MIA(IMP) holder

  •     The trial documentation required by the UK (IMP) holder

  •     How Sharp provides the UK QP oversight of these imports

Importer of Record (IOR) — Know what importer record means and its responsibilities? How will a supply chain be affected with the new QP oversight regulations introduced? What changes has Brexit brought when importing to the UK?

Join experts from Sharp, Lisa Parkhouse, Quality Manager / QP; and Stewart Howells, Logistics Team Manager, for the live webinar on Wednesday, March 9, 2022 at 9:30am EST (2:30pm GMT/UK).

For more information, or to register for this event, visit New Qualified Person Oversight Regulations When Importing Investigational Medicinal Product to the UK.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year, thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com

For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

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