11.120.01: Pharmaceutics in general

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  1. HISTORICAL

    DIN EN 1041▹ [ Withdrawn ]

    This document has been replaced. View the most recent version.

    Information supplied by the manufacturer of medical devices (includes Amendment A1:2013)

    standard by DIN-adopted European Standard, 12/01/2013 in English, German.

    Languages: English,German

    Historical Editions: DIN EN ISO 20417 (2022), DIN EN ISO 20417 (2021), DIN EN ISO 20417 - DRAFT (2019), DIN EN 1041/A1 - DRAFT (2013), DIN EN 1041 (2008)

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  2. HISTORICAL

    DIN EN 1041▹

    This document has been replaced. View the most recent version.

    Information supplied by the manufacturer of medical devices

    standard by DIN-adopted European Standard, 11/01/2008 in English, German.

    Languages: English,German

    Historical Editions: DIN EN ISO 20417 (2022), DIN EN ISO 20417 (2021), DIN EN ISO 20417 - DRAFT (2019), DIN EN 1041 (2013), DIN EN 1041/A1 - DRAFT (2013)

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  3. HISTORICAL

    DIN EN 1041/A1 - DRAFT▹

    This document has been replaced. View the most recent version.

    Draft Document - Information supplied by the manufacturer of medical devices; German version EN 1041:2008/FprA1:2013

    standard by DIN-adopted European Standard, 01/01/2013.

    Languages: German

    Historical Editions: DIN EN ISO 20417 (2022), DIN EN ISO 20417 (2021), DIN EN ISO 20417 - DRAFT (2019), DIN EN 1041 (2013), DIN EN 1041 (2008)

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  4. HISTORICAL

    DIN EN ISO 10993-14▹ [ Withdrawn ]

    This document has been replaced. View the most recent version.

    Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)

    standard by DIN-adopted European-adopted ISO Standard, 05/01/2002 in German, English.

    Languages: English,German

    Amendments, rulings, and supplements: DIN EN ISO 10993-14/A1 - DRAFT (2009)

    Historical Editions: DIN EN ISO 10993-14 (2009)

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  5. HISTORICAL

    DIN EN ISO 10993-16▹ [ Withdrawn ]

    This document has been replaced. View the most recent version.

    Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)

    standard by DIN-adopted European-adopted ISO Standard, 11/01/1997 in German, English.

    Languages: English,German

    Amendments, rulings, and supplements: DIN EN ISO 10993-16/A1 - DRAFT (2009)

    Historical Editions: DIN EN ISO 10993-16 (2018), DIN EN ISO 10993-16 - DRAFT (2016), DIN EN ISO 10993-16 (2010), DIN EN ISO 10993-16 (2009), DIN EN ISO 10993-16 - DRAFT (2008)

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  6. DIN EN 12442-1▹

    Animal tissues and their derivatives utilized in the manufacture of medical devices - Part 1: Analysis and management of risk; English version of DIN EN 12442-1

    standard by DIN-adopted European Standard, 01/01/2001 in English, German.

    Languages: English,German

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  7. DIN EN 12442-2▹

    Animal tissues and their derivatives utilized in the manufacture of medical devices - Part 2: Controls on sourcing, collection and handling; English version of DIN EN 12442-2

    standard by DIN-adopted European Standard, 01/01/2001 in English, German.

    Languages: English,German

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  8. DIN EN 12442-3▹ [ Withdrawn ]

    Animal tissue and their derivatives utilized in the manufacture of medical devices - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible agents; English version of DIN EN 12442-3

    standard by DIN-adopted European Standard, 01/01/2001 in English, German.

    Languages: English,German

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  9. HISTORICAL

    DIN EN ISO 13408-2▹ [ Withdrawn ]

    This document has been replaced. View the most recent version.

    Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)

    standard by DIN-adopted European-adopted ISO Standard, 09/01/2011 in German, English.

    Languages: English,German

    Historical Editions: DIN EN ISO 13408-2 (2018), DIN EN ISO 13408-2 - DRAFT (2017), DIN EN ISO 13408-2 - DRAFT (2011)

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  10. HISTORICAL

    DIN EN ISO 13408-2 - DRAFT▹ [ Withdrawn ]

    This document has been replaced. View the most recent version.

    Draft Document - Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003); German version FprEN ISO 13408-2:2010

    standard by DIN-adopted European-adopted ISO Standard, 01/01/2011.

    Languages: German

    Historical Editions: DIN EN ISO 13408-2 (2018), DIN EN ISO 13408-2 - DRAFT (2017), DIN EN ISO 13408-2 (2011)

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