We provide answers!

Is your documantation

compliant with directives?

Creating legally compliant documentation is both an obligation and a challenge for us. We’re a long-standing member of the tekom professional association and in the business for over 30 years – so we understand the dynamics of the industry. Protecting users has been a guiding ideal for EU directives. This has led to more and more regulations and made technical documentation a legal minefield.

Legal understanding is mandatory, especially for us as a service provider specialising in the review, creation and translation of technical documentation. Our professional knowledge is at your disposal to help your improve your documentation. We keep up to date with publications and lectures from the tekom association, and with our own analyses of guidelines and standards. Get in touch with us. We’ll write legally compliant technical documentation for you. We’d also be happy to check any of your existing texts.

Scriptor highlights

  • Free news updates for customers
  • Individualised advice and analysis
  • Detailed analyses by the association’s legal serviceList Title
  • Preparation and updates of documentation based on these analyses

Scriptor highlights

  • Free news updates for customers
  • Individualised advice and analysis
  • List TitleDetailed analyses by the association’s legal service
  • Preparation and updates of documentation based on these analyses

Your advantages

  • Scriptor finds out about new legal developments
  • Thematic and individualised legal service
  • Analysis and implementation from a single source

Your advantages

  • Scriptor finds out about new legal developments
  • Thematic and individualised legal service
  • Analysis and implementation from a single source

IEC 82079-1

The new ISO/IEC 82079-1 standard provides more precise specifications for the design of operating/user manuals for consumers and B2B. It also defines quality criteria for the authoring process

Machinery Directive 2006/42/EC

As an EU directive, the Machinery Directive 2006/42/EC has a quasi-legislative status. Manufacturers must comply, and this compliance is monitored by national surveillance authorities. The Machinery Directive

MDR + IVDR 2017/746

The European Medical Device Regulation (MDR) 2017-745 and the in-vitro Diagnostic Medical Devices Regulation (IVDR) 2017-746 must be implemented by manufacturers …

ANSI Z535.6

In accordance with the German Product Liability Act (ProdHaftG), a main task of user documentation is to make residual risks of a product recognisable to the user and to provide appropriate instructions …

Directive 2014/35/EU

Since April 2016, the Low Voltage Directive 2014/35/EU is valid for electrical equipment in a range of 50 to 1000 volts for alternating current and 75 to 1500 volts for direct current. …