FMEA and PLP

Work towards Total Quality Management
with FMEA and PLP based on SAP!

SAP Quality Management

FMEA and PLP

In order for companies to remain competitive in the future, it is especially important that they can continue to achieve improvements in quality. Of especial importance here is defect minimisation and the reduction of lifecycle costs that rise with each step along the supply chain. The continuous quality improvement process should also be supported by a software-based system.


Thanks to its centralised management and maintenance of master data, FMEA with SAP offers the advantage that this data can be used universally. This avoids having separate interfaces to external software and solutions, which in turn guarantees data integrity, ensuring that the information is completely free of redundancy.

Alongside integration with Complaints Management, the utilisation of the same authorisation model for all components and the consistent linking to FMEA within production control plans ensures that data is up-to-date at all times, thereby minimising errors that would otherwise result from outdated or inconsistent data.

The production control plan is primarily intended to control the quality process. This means the plan contains inspection procedures and tools and also inspection frequencies for the product/process characteristics applied from the FMEA system, to provide an optimum level of control for quality.

Thanks to the integrated IT solution with SAP, both communication and knowledge management along the supply chain can be simplified and improved over the long term.

If one considers the future viability of SAP QM functions, which are subject to continuous improvement, a decision to implement FMEA and PLP on the basis of a SAP system is a promising course to chart towards Total Quality Management.


WHY CHOOSE DHC?

Use our experience as specialists for FMEA and PLP with SAP QM

  • Over 20 years of expertise in the implementation of quality management with SAP, as well as the conceptual design of QM, QC and QA processes
  • Long-standing collaboration with SAP as a partner specialising in QM
  • Quality management know-how spanning several industries
  • A wealth of expertise in regulatory requirements
Germany
Matthias Bothe

Managing Director & Industry Unit Manager
Life Sciences, Chemie and Medical Engineering
phone: +49 681 93 666 0
email: matthias.bothe@dhc-gmbh.com

Matthias Bothe, DHC GmbH
Switzerland
Carsten Buri

Director Sales & Marketing
phone: +41 44 500 888 7
email: carsten.buri@dhc-ag.ch

Carsten Buri, DHC AG
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WEBINARS AND EVENTS

28. Januar
Web session (in German)

Validation of SAP S/4HANA on-premise and Private Cloud Edition

The webinar looks at the validation requirements for SAP S/4HANA on-premise vs. cloud systems.

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04. Februar
Web session (in German)

UDI: Implementing global requirements with the right strategy and software

Implementation of the UDI requirements based on the SAP Cloud Platform with the UDI Platform of p36

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10. Februar
Web session (in German)

Your journey to the secure Microsoft Cloud for Pharma, Medical Technology and Biotech

Overview of the key success factors for security on the path of regulated companies to the Microsoft Cloud

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11. Februar
Web session (in German)

New ISPE GAMP® Good Practice Guide: Enabling Innovation

What does the new ISPE Guide mean for Computer System Validation (CSV) or Computer Software Assurance (CSA)?

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18. Februar
Web session (in German)

QM in S/4HANA – Example of an integrated LIMS in a Customer Project

Presentation of the quality-relevant processes of a LIMS in a customer project with the help of SAP QM as an integrated overall solution.

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10. März
Web session (in German)

SAP S/4HANA Implementation and Validation in Life Sciences

Find out what benefits the LSA approach offers you for the optimal, validated deployment of S/4HANA.

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