VDI Standardisation Work - Principles and procedures

Medical Grade Plastics (MGP)

Human exposure to mechanical vibrations - Whole-body vibration

Human exposure to mechanical vibrations - Whole-body vibration - Corrigendum concerning standard VDI 2057 Part 1:2017-08

Human exposure to mechanical vibrations - Hand-arm vibration

Cleanroom technology - Cleanliness of medical devices in the manufacturing process

Cleanroom technology - Extractable soluble residue testing - Method for determining the actual condition and limit value testing

Maximum ambient concentrations referring to human health - Maximum ambient concentrations for nitrogen dioxide

Maximum immission values referring to human health - Maximum immission concentrations for ozone

Catalogues in maintenance and management of medical devices - Fundamentals

Vacuum coating quality assurance - Characteristics, applications and procedures

Vacuum coating quality assurance - Demands on plastics to be coated

Vacuum coating quality assurance - Production sequence and job steps

Vacuum coating quality assurance - Testing of vacuum coated plastics

Protective measures against vibration effects on man

Optical coherence tomography (OCT) - Process descriptions

Reprocessing hazards - Risk management in reprocessing of medical devices - Measures for risk control

Reprocessing hazards - Risk management in reprocessing of medical devices - Trainings

Hazards in medical areas - Risks of detectable surface changes on invasive medical devices - Measures for risk control

Biomaterials in medicine - Classification, requirements, and applications

Medical device software - Medical SPICE Process assessment model

Medical device software - Medical SPICE - Qualification of developers and assessors

Medical device software - Medical SPICE - Recommendations for software development

Systematical development for a model-based testing of medical devices - Fundamentals

Digital process chains in industrial medical technology - Production of custom-made devices

Management of hygienically relevant surfaces in medical facilities - Classification and design of hygienically relevant surfaces - Classification

Management of hygienically relevant surfaces in medical facilities - Classification and design of hygienically relevant surfaces - Design notes for different risk classes

Retesting of active medical devices in medical use - Testing principles

Biofabrication - Bioprinting - Printing process

Licensing and implementing of new nanotechnologies in the area of medical technology - Fundamentals

Sustainability in the construction and operation of hospitals - Fundamentals

Water heating systems - Comfort criteria and performance levels for planning, evaluation and implementation

Barrier-free buildings - Requirements and fundamentals

Barrier-free buildings - Aspects of sanitary installation

Barrier-free buildings - Aspects of electrical installation and building automation

Ventilation and indoor-air quality - Hygiene requirements for ventilation and air-conditioning systems and units (VDI Ventilation Code of Practice)

Ventilation and indoor-air quality - Hygiene requirements for ventilation and air-conditioning systems and units (VDI Ventilation Code of Practice) - Corrigendum concerning standard VDI 6022 Part 1:2018-01

Ventilation and indoor-air quality - Hygiene requirements for ventilation and air-conditioning systems and units - Special features of decentralised ventilation systems/units (VDI Ventilation Code of Practice)

Ventilation and indoor-air quality - Avoidance of allergenic exposure - Requirements regarding the testing and evaluation of technical products and components affecting the indoor air

Ventilation and indoor-air quality - Branch-specific guides - Waste treatment plants

Hygiene in drinking-water supply systems - Requirements for planning, execution, operation, and maintenance

Hygiene in drinking-water supply systems - Professional trainings in drinking-water hygiene

Technical good manufacturing practice - Application guideline for projects in the GMP environment

3rd-Party GMP Audits - Supplier audits in the pharmaceutical industry

Data management for life sciences

Project engineer - Knowledge profile

Project engineer - Requirements for qualification

Project engineer in projects with external team members - Knowledge profile

Project engineer in projects with external team members - Requirements for qualification