We would love to connect with you during the DIA and discuss how we can support you to optimise your path to market approval.

Working together we can:

  • Accelerate your drug development program to reduce your time to approval
  • Optimise the management of the regulatory process to provide accurate and predictable outcomes
  • Reduce your risks and increase the probability of gaining Market Authorization

Don't miss our  great speakers sharing their knowledge in different forums throughout the conference:


Dr Steffen Thirstrup - NDA Advisory Board Director & John Ellis, Communications Coach, PharmApprove, NDA Group

A tutorial on Tuesday, June 22 • 09:30 – 12:30 EDT – Tutorial (Short Course)

025A: #025A: Optimizing your interaction with EU Regulatory Authorities: How to Prepare and Perform


Shelley Gandhi, Patient Safety & Pharmacovigilance Director, NDA Group

A session on 17th June • 12:00 - 13:00 EDT  On-Demand and will be available anytime for viewing

OD: Safety Compliance

Clinical Trial Regulation is an Opportunity to Revisit Compliance at the Pharmacovigilance and GCP Interface


Dr Brian Edwards, Principal Consultant, NDA Group

Two Sessions - Semi-Live and will include live Q&A with our Speakers.

Monday, June 28 • 16:00 - 17:00 EDT
#SL: A Journey of Interdisciplinary Collaboration to Improve Safety Evaluation in Drug Development

Tuesday, June 29 • 14:00 - 15:00 EDT

#L: Systems Thinking: A better Way of Safety Management Planning


Click here to download the full programme.


 

To book a meeting with one our team simply
contact us meet-us@ndareg.com

Speakers

Dr Steffen Thirstrup

Advisory Board Director

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John Ellis

Communications Coach, PharmApprove

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Shelley Ghandi

Patient Safety & Pharmacovigilance Director

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Dr Brian Edwards

Principal Consultant

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Your drug development needs are unique

Contact us to learn how our experts can support you to meet all regulatory, quality and safety requirements and ensure the best path to approval.

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