Before launching clinical trials in EU countries, know exactly what you’re getting into. This guide, painstakingly compiled by the editors of the newsletter Clinical Trials Advisor, reviews the requirements of each of the EU countries and includes web references and complete legislative and regulatory texts where available.

The EU Clinical Trials Regulatory Reference Guide is an essential resource for anyone sponsoring trials in the EU.

Place your order today and you’ll receive:

• Fees, deadlines and other requirements for submitting applications to conduct clinical trials in the EU member states
• Agency contact information for the bodies that oversee clinical trials in the EU
• Ethics committee and informed consent requirements for conducting trials in the EU
• Routine and priority reporting requirements for each EU country
• And much more

Buy Now!

Get everything you need to conduct clinical trials in Europe with the EU Clinical Trials Regulatory Reference Guide. Priced at just $357, this invaluable reference is available in print or PDF format.

Satisfaction Guaranteed
There's no risk when you purchase from FDAnews with our money-back guarantee. Not satisfied with your publication? Return the hard copy within 30 days (in resalable condition), and we will refund 100 percent of your purchase price (less shipping/handling). For the electronic version, you must notify FDAnews within 24 hours of receipt of purchase to receive a refund.