MedDRA. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) developed...

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  • MedDRA
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    Created page with "The Medical Dictionary for Regulatory Activities was created for the purpose maintaining up-to-date terminology in regards to regulation of pharmacology, vaccines and things a..." New page The Medical Dictionary for Regulatory Activities...

  • Quintiles is the world’s leading provider of biopharmaceutical services. With a network of more than 27,000 professionals working in more than 80 countries, we have helped develop or commercialize all of the top 50 best selling drugs on the market...

  • Updated: Updated literature reference list Overview MHRA uses the E2B messaging standard to send and receive information on adverse drug reactions (ADRs) reported by patients and healthcare professionals. E2B is the mandatory messaging standard that...

  • Notes from the Field: Administration Error Involving a Meningococcal Conjugate Vaccine — United States, March 1, 2010–September 22, 2015 | MMWR MMWR Weekly Vol. 65, No. 6 February 19, 2016 PDF of this issue Notes from the Field: Administration Error...

  • At this year’s DIA e-Regulatory and Intelligence conference, one message was delivered over and over again about IDMP: Only 20-40% of the information that will go into IDMP will be found in existing structured databases. Where is the rest? In unstructured...

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  • Schedule | MedDRA

    The description, training materials and online registration form for each training event are available from the schedule below by clicking on the convenient event. NOTE: Face-to-Face classes are po...

  • MedDRA

    Send as e-mail Welcome to MedDRA In the late 1990s, the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) developed MedDRA, a ...

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