MoniDoseQMS presented at Healthtech Finland's eQMS working group meeting
On 19 May 2026, MoniDose Oy presented MoniDoseQMS to Healthtech Finland's Medical Device working group at a joint eQMS meeting in Helsinki — an English-language walkthrough of the platform and its free regulatory tools, shown from the user's perspective.
By MoniDoseQMS Team
On 19 May 2026, MoniDoseQMS was presented at the joint eQMS meeting of Healthtech Finland's Medical Device (MD) working group, held at Eteläranta 10 in Helsinki and streamed online via Teams. Alaa Salonen of MoniDose Oy gave the closing session of the afternoon — an English-language walkthrough of the platform from 15:40 to 16:00.
About the meeting
The MD working group, organised by Healthtech Finland (Terveysteknologia ry), is an open meeting place for medical device professionals. This session focused on electronic Quality Management Systems in the MDR and IVDR regulatory context. Several eQMS platforms were demonstrated back to back, each shown from the user's perspective — so attendees could see how the systems actually feel in everyday quality work, not just on a feature list.
What we showed
MoniDose Oy introduced MoniDoseQMS as a single platform that replaces a patchwork of disconnected tools: 130 integrated modules across 13 categories, covering ISO 13485, EU MDR, FDA QMSR, the EU AI Act, and more. In keeping with the meeting's theme, the platform was presented from the user's perspective — how a quality team works through document control, CAPA, audits, and training day to day.
The session also highlighted three free, interactive tools that anyone can use today — no account, no sales call, nothing to install. Here is a closer look at each.
Device Classification Wizard
Answer a short series of plain-language questions and the wizard shows where your device lands under EU MDR 2017/745 and the FDA framework, along with the likely conformity assessment or clearance pathway.
Startup Launchpad
For teams taking a regulated product to market, the Launchpad breaks the journey into milestones — from concept and research through design, risk management, testing, clinical evidence, and submission — with realistic cost and timeline ranges and a downloadable roadmap.
Regulatory Guide
Select your product type and target markets, and the Regulatory Guide assembles the applicable regulations and standards, estimated submission costs, the documents you will need, an audit-readiness view, and the MoniDoseQMS modules mapped to each requirement.
Couldn't make the meeting?
You can explore the same platform and tools online at any time. Try the free tools above, or book a personalised walkthrough with our team.