Skip to content
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

From design to field feedback.

Product stages
Record contents

Records added
at each stage.

  1. Requirements recorded
  2. Build linked to tests
  3. Release decision captured
  4. Field findings connected
  5. Change assessment prepared
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 complaint intake, assessment, report preparation, corrective actions and trend review in one governed workflow.

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

Product Lifecycle Management

Link requirements, risks, design outputs, verification and changes into a connected device record.

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

Software as a Medical Device

Connect software changes to requirements, risk controls, verification and release evidence, with human approval before deployment.

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.

From requirement to 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 programmes, 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
A clear starting point

Your questions, answered.

Where should we start?

Start with one of the three workflows and discuss the records, users, integrations and approval gates your team needs.

Who approves decisions and releases?

Your designated reviewers retain responsibility for regulatory, quality, clinical and release decisions. Software can help organise evidence and prepare drafts.

Does this cover every Life Sciences process?

The initial offering focuses on three MedTech workflows. Other Life Sciences needs should be scoped separately.