Speaker Engagements

April 2025

RareGeniX Panel Discussion and Networking Event, hosted by cpl Life Sciences & TOPRA at The Royal Society of Chemistry, London.

The RareGeniX team discussed the latest hot topics in Quality, Manufacturing, Regulatory, Patient Engagement and Clinical Considerations to Accelerate New Medicines to the Clinic. Thank you to our sponsors and collaborators cpl Life Sciences and TOPRA and all attendees for making this entertaining debate, fresh, energetic and fun!

June 2025

RareGeniX’s Chief Medical Officer Dr Dmitry Zamoryakhin and Patient Engagement Lead Keith Berelowitz met new and existing clients at BIO International, Boston.

Subscribe to our Linked In page to find out where you can meet us in person or simply email info@RareGeniXConsulting.com

Sep 2025

RareGeniX’s patient engagement lead Keith Berelowitz spoke at Patient Empowerment 25 alongside MHRA’s Chief Executive Office Lawrence Tallon

Oct 2025

TOPRA Symposium in Berlin, Germany.

RareGeniX’s Dr Dima Al Hadithi, Dr Christine Grew and Keith Berelowitz led a panel discussion alongside regulators from Germany & EMA [Dr. Ralf Sanzenbacher (PEI), Dr. Jens Reinhardt (European Medicines Agency)] to deliver a human medicines discussion entitled ‘From Barrier to Bridge: Practical Strategies for Successful Advanced Therapy Medicinal Product (ATMP) Development’ providing actionable insights for those developing ATMPs.

Nov 2025

CMC Partner Dima Al Hadithi’s spoke at GenScript’s Biotech Global Forum advancing dialogue on regulatory, CMC, clinical development and investment in the field of advanced therapies.

A great write up of the session in Pharmaceutical Technology Early planning, outsourcing and digitalisation to break down CGT CMC barriers – Pharmaceutical Technology

Read Article

Nov 2025

RareGenix’s Quality Partner Ian Pardo spoke at “GMP meets Development – GMP and FDA Compliance in Pharmaceutical
Development and IMP Manufacturing” in Heidelberg.

Ian delivered three sessions on

– Qualification and Validation for IMPs

– Cleaning Validation in
Pharmaceutical Development

– A Data Integrity Deep Dive Workshop focused on ALCOA+ in day-to-day operations and audit/inspection practice.