Event Time: 8:00 AM-12:30 PM EST (U.S. Washington, DC) // 1:00-5:30 PM GMT (London, UK)
Cost: $130 USD
Registration Deadline: February 1
The aim of this workshop is to highlight the advantages of collaboration between major pharmacopeias through applying Analytical Quality by Design and enhanced Analytical Method Lifecycle concepts. Diversity in the application of these concepts at a contextual stage can be a key motivator for wider engagement and knowledge transfer throughout the industry.
Speakers from industry, ICH Expert Working Group, the Medicines and Healthcare products Regulatory Agency (MHRA), U.S. Pharmacopeia (USP) and the British Pharmacopoeia (BP) will discuss the significant strides being taken around AQbD and the Analytical Method Lifecycle. This webinar includes reviews of practical case studies, experiences of members of respective pharmacopeial expert groups, regulator views on the developing science and an update on the application of ICH Q12. A group panel discussion will wrap up proceedings.
Questions? Please email firstname.lastname@example.org.