At YDL, we recognize that working with knowledgeable and experienced team is the most

valuable asset we can offer to our clients.


To fully complement our portfolio, we joined forces with one of the largest providers for Development Consulting, Regulatory Affairs, Quality Management & Compliance and Pharmacovigilance, Epidemiology, and Risk Management worldwide.


This partnership allows YDL to rely on a global team of experts with outstanding expertise in medicinal products and medical devices.


We offer a wide range of regulatory services, covering all stages of your product’s life-cycle:

  • Scientific Advice Meetings

  • Clinical Trial Applications

  • Marketing Authorisation Applications

  • PIL Authoring, Testing and Bridging

  • eCTD and NeeS Publishing & Submissions

  • Variations and Renewals


To learn more, please contact us