Showing 25–36 of 98 results Default sorting Sort by popularity Sort by average rating Sort by latest Sort by price: low to high Sort by price: high to low DDF4b Introduction to Informed Consent Forms €160.00 ex VAT Add to basket DDF50 – A Beginner’s Guide to Key Clinical Documents in the EU Drug Development Process €160.00 ex VAT Add to basket DDF54 Non-clinical study reports €160.00 ex VAT Add to basket DDF55 – Converting an Investigational New Drug (IND) application into an Investigational Medicinal Product Dossier (IMPD): process, regulatory requirements and potential pitfalls €160.00 ex VAT Add to basket DDF57 All clinical trials in Europe at your fingertips: Introduction to the public portal of the Clinical Trial Information System (CTIS) €160.00 ex VAT Add to basket EDG: Clinical Trial Transparency in Practice: Performance, Barriers, and the Emerging Role of AI €100.00 ex VAT Add to basket EDG: Controlling Complexity: Tools and Strategies to Improve the Efficiency of Cross-functional Reviews €100.00 ex VAT Add to basket EDG: High‐impact but Low‐visibility: Nonclinical Summary Writing for CTD Module 2 €100.00 ex VAT Add to basket EDG: How can medical writers positively impact rare disease documents? €100.00 ex VAT Add to basket EDG: Mastering the Rush: Exploring Practical Tools for Steering Complex Documents (eg, Protocols) with Large Cross-Functional Study Teams Under Tight Timelines €100.00 ex VAT Add to basket EDG: Medical Writing Peer Review of Clinical Trial Documents €100.00 ex VAT Add to basket EDG: Publication Ethics and Compliance €100.00 ex VAT Add to basket 1 2 3 4 5 6 7 8 9
