Medical device eQMS software without enterprise overhead

HAVGATE is eQMS software for medical device teams. Audits, CAPA, documents, training and suppliers sit in one system for ISO 13485, MDSAP, EU MDR and QMSR, without a long enterprise rollout. Built in Switzerland.

One eQMS, every quality process

The primary product is the medical device eQMS. Audit management, CAPA, document control, training and supplier quality each have their own page and their own records. They connect where the regulations connect: an audit finding can open a CAPA, a CAPA can change a controlled document, and that document can assign training. MDSAP's seven-chapter checklist is included, not bolted on as a PDF.

Built for the standards you are audited against

ISO 13485:2016 and ISO 9001:2015 are first-class audit criteria. MDSAP follows AU P0002.010. EU MDR is in the same engine for the QMS evidence you sample internally. FDA QMSR is the US quality-system regulation aligned with ISO 13485, so teams are not keeping a second conflicting checklist. Starter audits one standard at a time. Pro and above can combine them in one session.

From finding to CAPA to closure

The report is not the end of the audit. HAVGATE keeps the clause or MDSAP task on the finding, the nonconformance on the finding, and the effectiveness check on the CAPA. Root-cause tools are 5 Whys and Fishbone. A person approves the cause and the report. Drafting assistance does not sign for you.

Platform modules for medtech and other industries

CRM, inventory and bookkeeping are separate platform modules. Medical device teams can run them beside the eQMS, and companies outside medtech can use the same modules without buying quality software. A sales pipeline is not a device history record, and an invoice is not a CAPA. See the platform overview for what is available and what stays separate from the quality record.

Custom software and AI

Custom websites, business systems, AI automation and mobile apps are a second offer, delivered as services. They are not the homepage product and they are not the eQMS. Start at the services overview or the solutions catalog if that is the work you need.

Security, without invented certificates

The company is based at Utigenstrasse 7 in Central Switzerland. The security page states that product data is stored on Lovable Cloud in AWS US regions, with AES-256 at rest and TLS 1.3 in transit, on infrastructure from providers that publish SOC 2 Type II. Customer content is not used to train models. Read that page before you copy a sentence into a supplier questionnaire.

Pricing and the free trial

The audit platform is live and can be purchased. Starter is 19 a month, Pro is 39, Business is 89, and Enterprise is custom. The same face value is billed in USD, EUR, GBP or CHF. The audit trial is 14 days, needs no credit card, and includes up to 3 audit reports. Those prices and the trial are for the audit platform only.

Can we start with audits only?

Yes. The published plans and the free trial are the audit platform, which is live and can be purchased. They do not price CRM, inventory, bookkeeping, or the other quality modules.

Where is the sample report?

The fictional sample audit report AR-000101 is on the sample report page. It is not a customer deliverable.

Do platform modules and custom software replace the eQMS?

No. The eQMS is the primary product. Platform modules are a separate band for CRM, inventory and bookkeeping, including for companies that are not medical device manufacturers. Custom software and AI are a services offer on their own pages.