Webinar Recording: EU Regulatory Submission Timelines
As part of our Navigating EU Product Launch Milestones Webinar Series our expert speaker Brian Lavery, Regulatory Affairs Lead, Almac Group, shared his knowledge and experience of various EU regulatory filing options focusing primarily on the centralised procedure. Brian highlighted the criteria an applicant must meet, highlighted the key information required for submission and identified critical time points throughout the centralised procedure process.
This webinar recording will help you navigate the various EU regulatory filing options to allow you to plan ahead and save time in what can be a lengthy and complicated process.
Commercial Services
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.