Our Experts

At NDA we’re a team of experts – experts in the regulated disciplines, and experts in drug development.

Some of us have attained our experience from working inside regulatory authorities, carefully assessing the benefits and risks of new treatments. Some of us have worked for years in the biotech and pharmaceutical industry, patiently developing life changing products for patients suffering from debilitating and sometimes deadly diseases and conditions.

Whatever our background, we share a passion for the art and science of drug development and for making a difference to the clients and the patients we ultimately serve.

Get to know the people behind the passion – read more about our incredible team below.

All services Development Strategy Medical Devices Pharmacovigilance Strategic Communications Regulatory Quality & Compliance NDA Advisory Board
All expertise Oncology Vaccine Immunogenicity HTA In-Vitro Diagnostics Non-Clinical Cell and Gene Therapy Paediatric Clinical CMC Market Access Rare Disease ATMP Cardiology Biostatistics Acceleration Strategies Medical Devices Patient Safety Quality Bioanalysis
01-10-2020

Dr Mel Walker

Advisory Board Member
Expert in commercial strategy, market access, pricing and reimbursement
Read More
01-10-2020

Dr Thomas Lönngren

Strategic Advisor
Expert in the EU regulatory system and global regulatory strategies
Read More
01-10-2020

Dr Yngve Mikkelsen

Advisory Board Member
Expert in development strategy, market access, HTA and reimbursement
Read More
01-10-2020

Professor Carole Longson

Advisory Board Member
Expert in Science policy, market access, pricing and reimbursement
Read More

Contact Us

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.

Let's Bring Medicines to the World

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