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  2. Federal Department of Foreign Affairs - Wikipedia

    en.wikipedia.org/wiki/Federal_Department_of...

    The FDFA has been one of the key Swiss ministries since the creation of the modern Swiss federal state in 1848. Originally, what was then known as the "Federal Political Department" (FPD) was led by whomever held the rotating presidency, meaning the responsibility for foreign affairs changed on a yearly basis. With very limited means at its ...

  3. Federal administration of Switzerland - Wikipedia

    en.wikipedia.org/wiki/Federal_administration_of...

    The Federal Department of Foreign Affairs (FDFA) is Switzerland's ministry of foreign affairs. As of 2019, it is headed by Ignazio Cassis ( FDP/PRD ). It is composed of the General Secretariat and of the State Secretariat, which in turn is composed of the following directorates and agencies: [ 12 ]

  4. Electronic common technical document - Wikipedia

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

    A high level folder structure (required) An XML "backbone" file that provides metadata about content files and lifecycle instructions for the receiving system; An optional lower level folder structure (recommended folder names are provided in Appendix 4 of the eCTD specification) Associated document type definitions (DTDs) and stylesheets.

  5. ICD-10 Procedure Coding System - Wikipedia

    en.wikipedia.org/wiki/ICD-10_Procedure_Coding_System

    The ICD-10 Procedure Coding System (ICD-10-PCS) is a US system of medical classification used for procedural coding.The Centers for Medicare and Medicaid Services, the agency responsible for maintaining the inpatient procedure code set in the U.S., contracted with 3M Health Information Systems in 1995 to design and then develop a procedure classification system to replace Volume 3 of ICD-9-CM.

  6. Investigational New Drug - Wikipedia

    en.wikipedia.org/wiki/Investigational_new_drug

    The United States Food and Drug Administration's Investigational New Drug (IND) program is the means by which a pharmaceutical company obtains permission to start human clinical trials and to ship an experimental drug across state lines (usually to clinical investigators) before a marketing application for the drug has been approved.

  7. Helene Budliger Artieda - Wikipedia

    en.wikipedia.org/wiki/Helene_Budliger_Artieda

    From 1 July 2006 to 2008, Budliger Artieda was Head of Finance at the FDFA. [1] In 2008, Foreign Minister Micheline Calmy-Rey appointed Helen Budliger Artieda as the first female director of the FDFA. On 1 October 2008, Budliger Artieda took over the Directorate for Resources at the FDFA from Martin Dahinden, [1] who became head of the SDC ...

  8. Structured Product Labeling - Wikipedia

    en.wikipedia.org/wiki/Structured_Product_Labeling

    Structured Product Labeling (SPL) is a Health Level Seven International (HL7) standard which defines the content of human prescription drug labeling in an XML format. [1] The "drug labeling" includes all published material accompanying a drug, such as the Prescribing Information which contains a great deal of detailed information about the drug.

  9. Common Technical Document - Wikipedia

    en.wikipedia.org/wiki/Common_Technical_Document

    The CTD is an internationally agreed format for the preparation of applications regarding new drugs intended to be submitted to regional regulatory authorities in participating countries.