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Essentra Packaging webinars highlight regulatory challenges in clinical trials packaging

Label Solutions Packaging Solutions

Essentra Packaging is to host a free series of industry webinars to help packaging professionals find practical and effective solutions to the labelling of clinical trials, against the backdrop of complex regulatory change.

Titled, ‘The implications on Clinical Trials labelling due to Annex VI changes and patientricity’ the first webinar in the series takes place on 2 December at 15:00 GMT with interested parties invited to register online for the event.

As well as highlighting ways of dealing with the new labelling demands required under Annex VI of thee Clinical Trials Regulation (Regulation (EU) No 536/2014), members of the Essentra Packaging team will provide guidance and advice to attendees around patientricity. Topics to be covered include direct to patient implications, market challenges including those presented from the pandemic, and what successful secondary packaging solutions exist to help improve patient safety.

‘Annex VI will inevitably add more complexity to what is already a highly regulated sector and those involved in clinical trial labelling need solutions,’ said Diarmuid Wilson, business development director UK and Ireland at Essentra Packaging.

‘In what will be a highly informative, and approachable session our first webinar will aim to provide guidance to those across the pharmaceutical and clinical trials sector.’

Essentra Packaging will also showcase a series of successful case studies during the event, showing how it has supported customers to implement effective clinical trial solutions. The 60 minute session will end with a questions and answers session where attendees will have the ability to ask questions in relation to the regulation and requirements for packaging.

Those interested in attending the event should complete this registration form.


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