New standards for Investigational Medicinal Products (IMP) in clinical trials (online)

GS1 standards for identification in clinical trials

  • TBD

1 day course

English

1.000,- DKK ex VAT
(app. 134,- EUR ex VAT)
50% DISCOUNT FOR PUBLIC INSTITUTIONS

At the moment there are no available dates for this course.

Summary

This 2-hour online course (13-15 CET) provides you with knowledge about the new GS1 standards for IMP. Also, world leading experts from industry and healthcare make the case for why standardisation in the clinical trial area is so important: a pharmaceutical company presents why they decided to implement the standards in their clinical trials, and you will hear from a site personnel perspective how standards and barcodes have impacted the resources required at site level and how they minimise the risk for errors.
 

Key words

  • GS1
  • Standards
  • Clinical trials
  • Barcodes
  • Investigational Medical Product (IMP)

What you will learn

  1.  The value of implementing standards in clinical trials for both safety and logistical efficiency
  2. The function of barcodes in optimising resources and minimising errors at site level
  3. The content of the GS1 standard

What your company will get

  1. An employee or stakeholder who understands the GS1 standard for IMP and the rationale for implementing it, including: full supply chain traceability; increased efficiency by having faster data compiling; and less time spent on validating data

WANT TO KNOW MORE ABOUT THIS COURSE?

Contact Coordinator Christina Spangsberg at +45 39 15 09 22

Send an email