Every regulatory project is unique—that’s why AAYT offers custom tailored quotes. Pricing is based on your development stage, regulatory requirements, and timelines—ensuring you only pay for the services that align with your needs.
Whether you require EU Legal Representation under the Clinical Trials Regulation (CTR), EMA designations, or full regulatory strategy support, our experienced regulatory affairs professionals deliver the most budget-friendly solution on the market.
We serve as your official EU designate—sharing legal responsibility when required and ensuring your compliance.
We act as your named contact in CTIS and with EU/EEA authorities for all regulatory communications.
Your EU regulatory needs are handled by senior regulatory professionals with deep CTR, EMA, and member state expertise.
We respond to regulatory and sponsor inquiries within 24 business hours to keep your timeline on track.
Track regulator communications, tasks, and milestones via a purpose-built project management system.
We ensure adherence to all relevant EU regulations and programs—providing full legal accountability where required.
Learn exactly what’s included in your quote and how quickly you’ll receive it. Here's how to proceed:
Risk-free engagement backed by our unmatched speed, precision, and value—if you’re not completely satisfied within 14 days, cancel for a full refund, no questions asked.
We’ll help you assess your readiness to appoint an EU Legal Representative, answer your questions, and explore your eligibility for EU incentives for small and medium-sized businesses, promising new medicines, and treatment of rare diseases.