Quintalys · Consulting & Technology Solutions

Quality & Regulatory Capability, Delivered as a Service

The global capability centre model changed how companies run IT and finance. Quintalys brings it to quality and regulatory operations. Your standard, repeatable Q&R processes are run by dedicated, trained teams in cost-effective delivery locations, around the clock, with senior EU-based oversight. You get capacity, speed and consistency without building it yourself.

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What we offer

Standard Q&R processes, run at scale

Much of the daily work in a quality and regulatory organisation is essential, repeatable and high-volume. It ties up skilled people and slows the business when it falls behind. We take on these processes as a managed service, combining our consulting expertise with our technology solutions, so your own team can focus on decisions, design and strategy. The areas below are typical examples, not a fixed menu.

Quality Operations

The routine running of your quality system: nonconformance and CAPA administration, change control, training records, internal audit scheduling and quality KPI reporting.

Documentation & Records

Document control and records management within your QMS: formatting, review and approval routing, periodic reviews, record retention and archiving.

Regulatory Operations

Keeping regulatory information complete and current: technical documentation upkeep, labelling and IFU checks, UDI and registration data, and renewals across markets.

Post-Market Operations

Complaint intake and processing, trending, vigilance tracking, literature screening and preparation of post-market reports for your review and sign-off.

Supplier & Product Quality Operations

Supplier files, certificates and agreements, review of acceptance and inspection records, and follow-up on supplier corrective actions.

Backlog Clearance & Record Clean-up

Extra hands for remediation and audit preparation: reviewing and scrubbing historical records, closing out old backlogs, and finding and fixing gaps before an auditor does.

Something else in mind?

If a quality or regulatory task is repeatable and well defined, we can most likely run it for you. Tell us what is taking up your team's time, and we will scope it together.

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How we work

Our approach

We work as an extension of your quality organisation, not a black box. Process ownership and quality decisions stay with you, consistent with your obligations for controlling outsourced processes under ISO 13485. Quintalys provides the governance, the senior review and a dedicated delivery team working inside your QMS and to your procedures. A hub-and-delivery-centre structure, standard work and clear service levels make the service predictable, scalable and audit-ready.

01
Scope & onboarding

We map the processes in scope, their volumes, systems and service levels, and agree a transition plan with you. Knowledge transfer runs alongside your team, with no disruption to day-to-day operations.

02
Transition & process setup

Each process is documented as standard work within your QMS, system access is set up, and the delivery team is trained on your products and procedures. A parallel-run period confirms quality before full handover.

03
Ongoing delivery & reporting

Work moves through a follow-the-sun model across time zones, so tasks progress while your own team is offline. Agreed service levels, KPI dashboards and regular governance reviews keep performance fully transparent.

04
Continuous improvement & review

We apply Lean Six Sigma methods to remove waste and variation, automate repetitive steps, and adjust scope as your needs change. The service becomes faster and more efficient over time.

Why Quintalys

What sets us apart

Capability-centre economics, senior-level quality
High-volume work is delivered from cost-effective locations, while senior EU-based experts review and sign off the outputs that matter. You pay for skilled capacity, not overhead.
Round-the-clock, follow-the-sun delivery
Delivery teams across time zones keep CAPAs, complaints and document changes moving around the clock, cutting cycle times and backlogs.
Scalable: ramp up or down as needed
Add capacity for a remediation project, a notified body audit or a new market launch, then scale back. No recruitment lead times and no fixed headcount.
Consistent, audit-ready, technology-enabled
Standard work, built-in senior review and full traceability inside your QMS, supported by AI-enabled tools for speed and accuracy. Every record is prepared to withstand notified body and regulatory scrutiny.

Ready to get started?

Tell us which processes are slowing your team down. We will show you what a Quintalys capability centre could take off your plate, and what it would save.

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