WHO clinical registry standards?

Interventions from clinical trials are a crucial component of healthcare. “Every clinical study must be recorded in a publicly accessible database before recruitment of the first subject,” the Declaration of Helsinki mandates. Establish a clinical registry to create a baseline data quality level, validate data, and improve universal access and Validity of research data. A clinical trial register is an official record of the clinical research’s minimal, globally agreed-upon quantity of data that is kept and maintained in a database.

Participating primary and partner registries must adhere to predetermined requirements to maintain data uniformity. These six essential standards are:

  • Content – The trial registration data set has 24 points that must be followed.
  • Quality and Validity – verifies the accuracy of the information registered and adherence to best practice guidelines.
  • Accessibility guarantees that database entries and information are available around the clock in both English and local languages.
  • Unambiguous Identification – assures trial registration only needs to be done once and offers an impressive trial identification number.
  • Technical Capacity – safeguards against corruption and data loss
  • Administration and Governance – Information on ownership and governance is available to the public. It also establishes a data transfer method in the event the registry cannot continue operating.

Author’s Update: Keep up to date on industry advancements, support, and training.

Pubrica Connect: Read articles about research, technology, and health communities daily.

Researcher Academy:Improve your manuscript by learning academic writing skills.

Language editing by Pubrica Author Services:Before submitting your work, double-check that it is written in proper English.

Translation by Pubrica Author Services: Translate your work into English professionally.

Search engine optimization (SEO): Make your article more visible by using SEO.

Your paper, your way: Save time by making your first submission simple.