White Paper

Clinical Trial Disclosure Compliance A Moving Target Due To Ever-Changing Global Regulations

Source: Citeline
Quality check mark iStock-1223732386

Ensuring clinical trial disclosure compliance remains a challenge for sponsors, irrespective of the number of trials they conduct or the countries involved. For sponsors with trial sites spanning multiple nations, the ever-evolving global regulations add complexity. This year alone, there have been 115 updates across global regulatory agencies, resulting in 59 updates to the TrialScope Intelligence database. These updates affect various countries, including Australia, Bosnia, Canada, Germany, India, Latvia, Panama, Peru, Serbia, Slovakia, Switzerland, and Thailand.

Common global disclosure updates encompass new guidance documents, newsletters (particularly from the European Medicines Agency due to the Clinical Trial Information System portal), and authority notifications. Regulatory agencies have been continuously refining disclosure rules, including significant developments in 2020 triggered by the COVID-19 pandemic and Brexit.

In the future, sponsors may need to address data anonymization from devices like mobile phones and wearables, possibly leading to more targeted regulations for data capture through such technologies. Review what other types of changes have occurred, where they were, and how they are implemented by accessing the white paper below.

access the White Paper!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.

Subscribe to Clinical Leader X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.

or

Subscribe to Clinical Leader