Currently eight of the ESR's in PEARRL are completing a secondment at one the Regulatory Partners organisation in PEARRL.
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Huge thanks to all our Regulatory partners for organizing these secondments.  Special thanks to Jobst Limberg (BfARM), Evangelos Kotzagiorgis (EMA), Sean Jones (MHRA and Una Moore (HPRA) as the coordinators of these regulatory-academia collaborations

Dr. Rodrigo Chrisfoletti, Division of Therapeutic Equivalence, Brazilian Health Surveillance Agency (ANVISA), presents a research presentation entitled 'Going beyond the traditional BE borders: using in vitro and in silico tools to improve the assessment and extrapolation of therapeutic equivalence'

The Academy of Pharmaceutical Sciences is hosting a joint meeting of Biopharmaceutics and Regulatory Science in London in November 2017.  The focus of the workshop is on 'Developing Clinically Relevant Dissolution Specifications for Oral Drug Products - Industrial and Regulatory Perspectives'. A very interesting programme is planned.  For further info see https://www.apsgb.co.uk/Events/20171107/Default.asp