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Product Launch Webinar: Regulatory Submission Strategies for EU27 & UK Product Launches

Throughout this webinar David shares his knowledge and experience of various EU regulatory filing options focusing primarily on the Centralised Procedure.

David highlights the criteria an applicant must meet, the key information required for submission and identify critical time points throughout the Centralised Procedure process.
Now that the UK has withdrawn from the EU, David also shares insight into the impact of Brexit on Regulatory Strategies. He provides guidance and share vital information on the best approach for you to gain approval in the UK post a positive CHMP opinion and EC decision.

This webinar will help you navigate the various EU & UK regulatory filing options to allow you to plan ahead and save time in what can be a lengthy and complicated process.

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Almac Pharma Services provide a wide range of customised commercial services from supporting product launch, manufacturing and / or packaging drug product, to securing supply chain with global serialisation solutions.

Our flexible, quality-led commercial solutions range from orphan drug launches to ongoing high-volume commercial product manufacture, packaging and supply.

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