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Life Sciences & MedTech · DeX

MedTech expertise, built into software.

Device records, software delivery and post-market workflows.

DeX delivery workspace Device records & release evidence
  1. Business brief
  2. Requirements
  3. Workflow build
  4. QA evidence
  5. Security
  6. Reviewer release
New DeX projectReady for review

Product & quality team · Illustrative projectWe need one connected device record, with evidence ready for every review.

  1. Requirements agentRequirements, risk links and review rules
    QueuedWorkingDoneSign-off
  2. Design agentDevice record and reviewer screens
    QueuedWorkingDoneSign-off
  3. Build agentEvidence links, records and integrations
    QueuedWorkingDoneSign-off
  4. QA agentTests from acceptance criteria
    QueuedWorkingDoneSign-off
  5. Security agentAccess, dependency and release checks
    QueuedWorkingDoneSign-off
  6. Deploy agentYour approved deployment environment
    QueuedWorkingDoneSign-off
Ready for your reviewers: approval before release

Human approval is part of the workflow. DeX prepares the evidence; your designated reviewers decide what is released.

The industry challenge

Time spent
reconstructing decisions.

Records that need reconciling
One connected workflow
Structured records with context
Evidence linked to requirements
Named reviewers and decisions
Findings feed controlled changes
Illustrative record connections
Across the lifecycle

Connect design with field feedback.

One connected device recordDesign, delivery and post-market
Field feedback returns to design

Findings become a reviewed change, linked to the original requirements.

Illustrative lifecycle
Three places to start

Choose the workflow
your team needs first.

Start with one process. Connect the wider lifecycle as your scope grows.

Post-market operations

Post-Market Compliance

Connect complaints, assessments, reports and corrective actions for review.

For your teamRegulatory affairs, quality assurance, complaints handlers and vigilance leads
Open full use case
Device lifecycle

Device Lifecycle Management

Link requirements, risks, design outputs and verification in one device record.

For your teamR&D, systems engineering, quality and regulatory teams
Open full use case
Software delivery

Medical Device Software

Link software changes to risk controls, test evidence and release approvals.

For your teamEngineering, product, QA, regulatory and clinical safety teams
Open full use case
Built with DeX

Your process becomes
a working software workflow.

Define the requirements, records and integrations before the build.

Build and release live software
  1. DescribeYour process, in plain language.
  2. RequirementsAgree the users, records and rules.
  3. WireframesSee the screens before the build.
  4. BuildConnect code, data and integrations.
  5. TestCheck against acceptance criteria.
  6. DeployReview the release before it goes live.
  7. SupportKeep pace with controlled changes.
Describe

The project brief

Connect device requirements, risks and test evidence. Give every release a named reviewer.

Brief captured
Illustrative delivery sequence.
Simon Christopher
Industry contact

Meet Simon Christopher.

Life Sciences & MedTech Industry Expert for DeX

Simon brings commercial and business-development experience across EMEA, with a focus on relationships, market entry and outcome-based client engagements. His industry experience spans Life Sciences account programs, medical-device
engineering services and MedTech/HealthTech market development.

Simon helps connect Life Sciences and MedTech customer needs with DeX delivery conversations, bringing commercial context, stakeholder relationships and partnership experience.

28 years across EMEAMedTech & HealthTechUK & EMEA partnerships
Meet Simon

FAQ

Which MedTech workflows are shown here?

This page presents product lifecycle management, software as a medical device delivery, and post-market operations. Each workflow page describes its own records, users and review gates.

How do we choose a starting workflow?

Choose the workflow closest to the process you need to improve. Bring the relevant records, current handoffs and required outputs so the team can define a bounded scope.

Who approves regulatory, clinical and release decisions?

Your designated regulatory, quality, clinical and release reviewers retain responsibility. The software organizes evidence and prepares drafts for those reviewers.

What is Simon Christopher's role on this page?

Simon provides the industry perspective for the MedTech workflows. His profile explains the experience and requirements context behind the work presented here.

What should we define before building?

Agree the intended users, source records, integrations, review gates and acceptance criteria for the selected workflow. Other Life Sciences processes need their own scope.