The paper aims to help deploy AR/VR technology in biopharma GxP environments. It also gives the areas of risk for IT professionals and users of these technologies at biopharma organizations to consider when developing the technology internally or implementing an off-the-shelf product.
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The purpose of this document and action plan is to articulate AR/VR hardware and software requirements; stimulate collaboration between biomanufacturers and vendors of AR/VR hardware and software and help vendors of AR/VR hardware and software construct roadmaps to unleash the potential of this technology in GMP environments.
BioPhorum member only content supporting the development of a publication on the industry requirements of AR/VR used in manufacturing and clean room requirements.