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Standards Worldwide
Standards Worldwide
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Medizintechnik

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Draft standard 2024-01

DIN 53010-1:2024-01 - Draft
Rheometry and Viscometry - Pharmaceutical, cosmetic and medical products/devices - Testing the rheological properties - Part 1: Determination of the viscoelastic behavior of semisolid preparations using an oscillatory rheometer by amplitude sweep

from 80.20 EUR VAT included

from 74.95 EUR VAT excluded

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Standard [CURRENT] 2023-04

DIN 61632:2023-04
Surgical dressings - Cotton crepe bandages

from 50.70 EUR VAT included

from 47.38 EUR VAT excluded

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Standard [CURRENT] 2023-12

DIN EN 13726:2023-12
Test methods for wound dressings - Aspects of absorption, moisture vapour transmission, waterproofness and extensibility; German version EN 13726:2023

from 174.20 EUR VAT included

from 162.80 EUR VAT excluded

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Standard [CURRENT] 2024-10

DIN EN 17854:2024-10
Antimicrobial wound dressings - Requirements and test method; German version EN 17854:2024

from 139.20 EUR VAT included

from 130.09 EUR VAT excluded

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Standard [CURRENT] 2023-07

DIN EN ISO 14375:2023-07
Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing (ISO 14375:2018); German version EN ISO 14375:2023

from 87.90 EUR VAT included

from 82.15 EUR VAT excluded

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Standard [CURRENT] 2024-11

DIN EN ISO 15378/A1:2024-11
Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) - Amendment 1: Climate action changes (ISO 15378:2017/Amd 1:2024); German version EN ISO 15378:2017/A1:2024

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Draft standard 2025-04

DIN EN ISO 22532:2025-04 - Draft
Health informatics - Identification of medicinal products - Core vocabulary (terms and definitions) for the IDMP Standards (ISO/DIS 22532:2025); German and English version prEN ISO 22532:2025

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Technical rule [CURRENT] 2024-03

VDI-EE 6306:2024-03
3rd-Party GMP Audits - Supplier audits in the pharmaceutical industry

The expert recommendation is intended to be applied for auditing outsourced activities in accordance with the EU GMP Guidelines. It serves as guidance for companies and auditors, providing minimum ...

from 79.10 EUR VAT included

from 73.93 EUR VAT excluded

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inhouse seminar

UDI – Anforderungen an Medizinprodukte und In-vitro-Diagnostika

This seminar can be booked in-house as an in-house seminar. Please contact us if you are interested in this offer.

In-house seminar at your location Get an offer

DIN Members receive 15 % discount

Technical rule [CURRENT] 2022-10

IWA 37-3:2022-10
Safety, security and sustainability of cannabis facilities and operations - Part 3: Good production practices (GPP)

from 227.80 EUR VAT included

from 212.90 EUR VAT excluded

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