Life Science PLM

Within the Life Science and Medical Devices sectors regulatory compliance work already claims large amounts of time and resources. With the current EU Medical Device Regulation, even stricter requirements will be imposed on quality management to ensure compliance.

The tools and processes within PLM can dramatically facilitate quality management system work, including by integrating product and process information, decision-making, and history. PLM work provides reliable support in the digitalization of clinical data and lays a solid foundation for regulatory compliance.

  • We can offer a broad spectrum of services and solutions within PLM to support regulatory compliance processes in both Life Science and Medical Devices.
  • We have extensive experience in developing and implementing customized modules for commercial PLM tools to support specific areas within the regulatory compliance process.

Regulatory compliance has never been easier.

Services we offer:

  • Support in the procurement process of PLM systems for Life Science
  • Pre-studies and strategy development for PLM within Life Science
  • PLM IT system development focusing on the Life Science industry
  • Digitalization and streamlining of regulatory processes

Contact

Pär Möllberg

Pär Möllberg

Business Area - Life Science PLM

  • es.gnireenignelautriv@grebllom.rap
  • 86 00 908-670

Our combined knowledge of our customers' processes and PLM systems enables us to deliver the best solutions.

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Contact us

12 22 02-13(0)64+es.gnireenignelautriv@ofnies.gnireenignelautriv@sreerac

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