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  2. 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.

  3. 2008 Chinese heparin adulteration - Wikipedia

    en.wikipedia.org/wiki/2008_Chinese_heparin...

    The raw material for the recalled heparin batches was processed in China from pig's intestines by the American pharmaceutical firm Scientific Protein Laboratories. [1] [2] [3] The U.S. Food and Drug Administration was quoted as stating that at least 81 deaths were believed to be linked to a raw heparin ingredient imported from the People's Republic of China, and that they had also received 785 ...

  4. Electronic common technical document - Wikipedia

    en.wikipedia.org/wiki/Electronic_Common...

    An additional Draft Implementation Guide was released in February 2015 [5] The ICH and the FDA released draft specifications and guides in April 2016, and on May 13 there was an ICH "teleconference" to discuss the guidance and any queries or clarifications that might be necessary.

  5. Common Technical Document - Wikipedia

    en.wikipedia.org/wiki/Common_Technical_Document

    The CTD is maintained by the International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). [1] [2] After the United States, European Union and Japan, the CTD was adopted by several other countries including Canada [3] and Switzerland. [1]

  6. Trial master file - Wikipedia

    en.wikipedia.org/wiki/Trial_master_file

    The International Conference on Harmonization (ICH) published a consolidated guidance for industry on Good Clinical Practice in 1996 with the objective of providing a unified standard for the European Union, Japan, and the United States of America to facilitate mutual acceptance of clinical data by the regulatory authorities in those jurisdictions.

  7. Eggs now qualify as ‘healthy’ food, FDA says: Here’s why

    www.aol.com/eggs-now-qualify-healthy-food...

    The U.S. Food and Drug Administration (FDA) now classifies eggs as a “healthy, nutrient-dense" food, according to a new proposed rule. Registered dietitians react to the change.

  8. 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 ...

  9. Expert Trainer Reveals How to Keep Cats Out of the Christmas ...

    www.aol.com/expert-trainer-reveals-keep-cats...

    9 Reasons You Should Keep Your Cat Out of the Christmas Tree. Keeping your cat out of the Christmas tree isn’t just a battle of wills; it’s a safety concern too.