Carmen Coxon, partner/product manager at the MHRA, will give a general overview of the new MHRA structure and explain the available products and services, followed by a Q&A session.

To get the most from Carmen’s visit, she has asked attendees to submit specific questions in advance so that she can seek information from subject expert colleagues at MHA before her visit. As you’ll appreciate, the regulatory field is broad, and Carmen won’t have answers to everything at her fingertips during the session. You can submit your questions when you register for the event.

Here is a broad list of topics which may help you to formulate your questions:

• Clinical Trials
• ILAP
• Licencing
• Devices
• NIBSC manufacturing facility and services (useful for those wishing to lyophilise any biological reagents)
• British Pharmacopeia
• Enforcement
• Policy