enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Electronic common technical document - Wikipedia

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

    The electronic common technical document (eCTD) is an interface and international specification for the pharmaceutical industry to agency transfer of regulatory information. The specification is based on the Common Technical Document (CTD) format and was developed by the International Council for Harmonisation (ICH) Multidisciplinary Group 2 ...

  3. List of Guidances for Statistics in Regulatory Affairs

    en.wikipedia.org/wiki/List_of_Guidances_for...

    EMA/199678/2016: Reflection paper on extrapolation of efficacy and safety in paediatric medicine development. [8] EMA/189724/2018: Reflection paper on the use of extrapolation in the development of medicines for paediatrics. [9] EMA/129698/2012: Concept paper on extrapolation of efficacy and safety in medicine development. [10]

  4. Common Technical Document - Wikipedia

    en.wikipedia.org/wiki/Common_Technical_Document

    The Common Technical Document (CTD) is a set of specifications for an application dossier for the registration of medicine, designed for use across Europe, Japan, the United States, and beyond. [ 1 ] Major Synopsis

  5. European Medicines Agency - Wikipedia

    en.wikipedia.org/wiki/European_Medicines_Agency

    The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency ( EMEA ).

  6. EudraLex - Wikipedia

    en.wikipedia.org/wiki/EudraLex

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Free Trade Agreements; European Single Market.

  7. The 50 men accused in mass rape of Gisèle Pelicot - AOL

    www.aol.com/50-men-accused-mass-rape-072159807.html

    Families scrambling for answers. Since September, the 50 men have appeared, one after the other, in front of the court in Avignon. Usually in rape cases character investigations can take several days.

  8. Trial master file - Wikipedia

    en.wikipedia.org/wiki/Trial_master_file

    The minimum essential documents that are required for the registration of pharmaceutical products designed for human use are specified in the document 'ICH Good Clinical Practices,' published in 1997 by the ICH [2] Example ICH essential documents that would be required in any US, EU or Japan based clinical trial would include: signed protocol ...

  9. Parents charged with abuse after child's botched circumcision ...

    www.aol.com/parents-charged-abuse-childs-botched...

    On Nov. 28, deputies responded the couple's home, charging documents show, after receiving a call from a Department of Families Services employee contacted by a hospital employee about a child ...