Ranulf Barman

Legal experience:

• Advised multiple clients on the impact of the UK's departure from the EU on their compliance with ongoing and future medical device & IVD regulations.*
• Advised numerous pharmaceutical clients across a broad range of regulatory matters including, early access schemes, clinical trial obligations, adverse event reporting and engagement with regulators.*
• Advised a diagnostics University spin-out on its IP licensing and manufacturing agreements.*
• Advised numerous global food and cosmetics companies on the compliance of their European labelling and product warnings.*

Government experience:

• Managed a UK MHRA team of compliance investigators to ensure the safety of medical devices and IVDs on the market.*
• Co-lead EU Competent Authority on Medical Devices ('CAMD') programme on the implementation of new EU Medical Devices and IVD Regulations.*

*Denotes experience from previous firm.