enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Good clinical practice - Wikipedia

    en.wikipedia.org/wiki/Good_clinical_practice

    GCP aims to ensure that the studies are scientifically authentic and that the clinical properties of the investigational product are properly documented. GCP guidelines [1] include protection of human rights for the subjects and volunteers in a clinical trial. It also provides assurance of the safety and efficacy of the newly developed compounds.

  3. Investigator's brochure - Wikipedia

    en.wikipedia.org/wiki/Investigator's_brochure

    Owing to the importance of the IB in maintaining the safety of human subjects in clinical trials, and as part of their guidance on good clinical practice (GCP), the U.S. Food and Drug Administration (FDA) has written regulatory codes and guidances for authoring the IB, and the International Conference on Harmonisation (ICH) has prepared a ...

  4. International Council for Harmonisation of Technical ...

    en.wikipedia.org/wiki/International_Council_for...

    In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.

  5. ISO 14155 - Wikipedia

    en.wikipedia.org/wiki/ISO_14155

    ISO 14155 Clinical investigation of medical devices for human subjects -- Good clinical practice. This international standard addresses good clinical practices for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the safety and performance of medical devices for regulatory purposes.

  6. Good Clinical Practice Directive - Wikipedia

    en.wikipedia.org/wiki/Good_Clinical_Practice...

    The Good Clinical Practice Directive (Directive 2005/28/EC of 8 April 2005 of the European Parliament and of the Council) lays down principles and detailed guidelines for good clinical practice as regards conducting clinical trials of medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products.

  7. Download, install, or uninstall AOL Desktop Gold

    help.aol.com/articles/aol-desktop-downloading...

    Learn how to download and install or uninstall the Desktop Gold software and if your computer meets the system requirements.

  8. Right to withdraw - Wikipedia

    en.wikipedia.org/wiki/Right_to_withdraw

    The right to withdraw is a concept in clinical research ethics that a study participant in a clinical trial has a right to end participation in that trial at will. According to ICH GCP guidelines, a person can withdraw from the research at any point in time and the participant is not required to reveal the reason for discontinuation.

  9. Who will win national championship game? Expert predictions ...

    www.aol.com/win-national-championship-game...

    Our college football experts talked Ohio State Buckeyes vs. Notre Dame Fighting Irish predictions and who will win the CFP national championship game.