Augmented Reality for Life Sciences

Remote Adviser Video Calling

Within life sciences industries, multi-site organisations waste a lot of time and money by struggling to get the correct people to the correct places. 

Remote adviser function allows a remote expert to use the on-board camera of the augmented reality headset to see what the local technician is seeing and to provide feed-back to them on next steps audibly, using onscreen mark-ups or sharing the experts screen while they are present and have their hands available to take the actions required to fix the problem.

Procedure Following

Augmented Reality allows you to set out clearly detailed work instructions to your technicians in a hands-free way while they are completing a task. The instructions can include text, images, video and real-time data.


Work instructions allow technicians to be trained much more quickly while reducing mistakes and providing tractability. They also assist workers in speeding up their process and reduce the need for looking up reference material.

Through AR, companies can streamline their processes and procedures in order to better manage their time and labour allocation

Ingredient Code Scanning

Ensure that the correct ingredients are used by allowing our system to scan and confirm that the code matched that listed on the batch file. Reducing simple errors can benefit your organisation significantly. The system integrates with your existing tracking tool so the operator requires no extra work.

GMP Compliance for Life Sciences

UtilityAR is experienced at working in validated areas and demonstrating compliance with validated systems. Our solution is designed to meet the following requirements

 

  • ISO 22716 Cosmetics

  • ISO 9001 Quality Management

  • ISO 13485 Medical devices -- Quality management systems

  • Data Integrity and Compliance With Drug cGMP; Questions and Answers Guidance for Industry” https://www.fda.gov/media/119267/download

  • 21 CFR Part 314 and Part 600. Application and licensing submission requirements for new and generic drug applicants.

  • 21 CFR Part 210.  Current Good Manufacturing Practice in Manufacturing Processing, packing, or Holding of Drugs.

  • 21 CFR Part 211.  Current Good Manufacturing Practice for Finished Pharmaceuticals.

 

For more on good practice on meeting GMP requires on validated systems, download our slide deck.

Request a Demo

Find out how you can apply UtilityAR solutions to your business. 

enquiries@utilityar.com

UTILITYAR SOLUTIONS

UtilityAR creates Augmented Reality Solutions for Industries like Pharmaceuticals, Manufacturing, Utilities, and Data Centres.

 

We understand the importance of ease of setup and use of the platform. This has been a focus in the design of the product and means that it is the easiest to integrate solution on the market.

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