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DELTA WAYS

Digital Transformation

DELTA WAYS

Companies expect digitalisation to increase process efficiency, minimise potential sources of error and ultimately reduce costs. The first step in achieving this is to analyse individual needs and requirements.

Digital Solutions

All standalone software must be validated according to the relevant requirements and standards. This includes software that is part of a medical device or is itself a medical device.

Software Validation

The digitalisation of business models often results in the digital representation of processes that remain analogue in nature. No "digitalisation" without "digitisation"!

Digital Process Optimization

Business Services

DELTA WAYS

Suppliers and manufacturers

in particular can benefit from a

QM system that meets the requirements of ISO 13485.

ISO 13485 Gap Analysis

Various players in the medical technology industry are

required to implement a quality management system to comply with regulations such as the

MDR, IVDR, and FDA.

ISO 13485 Certification

When selecting a new supplier, it is important to consider a number of criteria, all of which must be regulated within the QM system.

Supplier Qualification and Evaluation

The purchase of new machines and tools, or necessary refurbishment and modernisation work in production, involves significant investment costs.

MedTech Manufacturing Consulting

The development of cutting-edge technologies and products in a highly regulated sector characterises medical technology and makes working with companies in this industry

complex and exciting.

Vertical Sales MedTech

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DELTA WAYS GmbH

An der Anlage (neu) 6

D - 41812 Erkelenz-Keyenberg

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Delta MB Switzerland GmbH

Medical Device Consulting

Industriestrasse 3

CH - 8952 Schlieren

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