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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
  • On-demand Webinar

Demystifying a Pressure Equipment Directive Technical File

Compiling an effective databook and providing the correct technical information can involve rework and thus be a complex and daunting task. Gain clarity on the requirements from industry experts.

Pressurized equipment

Demystifying a Pressure Equipment Directive technical file

Compiling an effective databook and providing the correct technical information can involve rework and thus be a complex and daunting task. Gain clarity on the requirements from industry experts.

In order to gain authorization to apply the CE Mark, Pressure Equipment Directive (PED) manufacturers are usually required to collect all applicable information related to the pressure equipment and submit it to the Notified Body. Compiling an effective databook and providing the correct technical information can involve rework and thus be a complex and daunting task.

Speaker: Valerio Fruggiero

Moderator: Angelo Micco

Join this webinar to help get clarity on the following questions:

  • What is a technical file or databook?
  • What information should a technical file contain?
  • When is a design technical file applicable?
  • When is a manufacturing technical file applicable?
  • What is an appropriate format for a technical file?

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Streamline pressure equipment certification for EU

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