# Best Ideagen Quality Management alternatives for medical device companies (2026)

Source: https://bestqmssoftware.com/alternatives/ideagen-quality-alternatives/
By Tom Muller, updated October 5, 2026
Part of Best QMS Software (https://bestqmssoftware.com/). Method: https://bestqmssoftware.com/how-we-rank/



Ideagen Quality Management, formerly Q-Pulse, is a long-established, multi-industry QMS with a packaged setup for medical device companies. Device teams usually start comparing it with other systems for one of the reasons below. Here's what our evidence shows, which alternatives fit which situation, and when staying is the better call.

## Why teams look for Ideagen Quality Management alternatives

**Design controls are a sales claim.** Design control workflows, design history files, ISO 14971 risk management and vigilance reporting appear on the FastStart sales page but not in the help centre.[^id-faststart][^id-help-api] The documented risk module is a general business risk register.[^id-help-risk] We found no device history record, UDI or IEC 62304 features, and no Jira or Git integration.[^id-help-api]

**Contract defaults.** Unless the order form says otherwise, the standard agreement runs for 24 months and renews automatically for further 24-month periods unless you give 90 days' notice. At renewal you can't cut licences below half of the previous fees.[^id-mssa] Data is deleted after termination. You must extract it yourself beforehand, and any help is at Ideagen's discretion and cost.[^id-mssa] Large exports cost extra.[^id-gcloud]

**Price rises.** Ideagen may raise fees once a year, and its terms set no cap or index.[^id-mssa] Three G2 reviewers report steep rises: from about $4,300 to $9,000 a year over two years, a rise "without warning", and a contract price that tripled after a forced move to the cloud version.[^id-g2-hike-a][^id-g2-hike-b][^id-g2-hike-c] A 2026 Capterra reviewer says they were "forced into an overpriced SAAS model".[^id-capterra]

**Paid extras.** Validation packs cost £4,000 (IQ/OQ) or £9,320 (IQ/OQ/PQ), and a dedicated customer success manager adds 15–25% to licence fees.[^id-gcloud-price]

**The interface.** Full functionality has historically needed the Windows desktop client.[^id-gcloud] Many G2 reviewers describe the interface as dated, clunky or not intuitive, especially the desktop client and report building.[^id-g2]

**Small teams.** The pack is priced and sized for 15 licences, and contracts default to two years.[^id-faststart][^id-mssa]

## Which alternative fits your situation

### You want design controls and risk in the QMS: Greenlight Guru

[Greenlight Guru](/reviews/greenlight-guru/) builds quality software only for medical device companies.[^gg-pricing] Its product tour shows a design control matrix that links user needs, inputs, outputs, verification and validation, next to a risk matrix of hazards, hazardous situations and harms.[^gg-tour] Trace graphs flag missing links across design, risk and tests.[^gg-pd] Each release ships a Part 11 IQ protocol and completed OQ and PQ reports at no extra cost, and you can export quality records in standard formats without paying for services.[^gg-pricing] It publishes an entry price of $12,000 a year, with implementation quoted separately, and Vendr reports a median of $43,989 a year.[^gg-pricing][^gg-vendr] Its renewals aren't capped either: the agreement lets it raise fees at each renewal with 90 days' notice.[^gg-msa] Users report it is weak for BOMs and change requests, and there are no pharma GMP modules.[^gg-reddit-worth][^gg-pricing]

### You build software as a medical device: Matrix Requirements or Ketryx

[Matrix Requirements](/reviews/matrix-requirements/) documents configurable traceability rules and links issues to Jira, GitHub, GitLab and Azure DevOps.[^mx-trace][^mx-git] Its template package covers IEC 62304.[^mx-sxmd] You can start a Matrix Req trial yourself, without a credit card.[^mx-trial] Prices are published: three Matrix Req users plus ten Matrix Quality licences come to about $21,800 a year.[^mx-list2026][^mx-quality] Supplier, audit and nonconformance workflows need Matrix Quality, a separate Salesforce-based product.[^mx-quality]

[Ketryx](/reviews/ketryx/) syncs requirements, software items, tests and risks from Jira, Git and test tools and generates the design history file from them.[^kx-dhf] It offers a 30-day self-serve trial, but paid plans are contact-sales.[^kx-signup][^kx-pricing] We found no documented supplier, internal audit or production record workflows, so most device companies will run it next to another eQMS.[^kx-llms]

### Your SOPs live in Word and you want services in one price: SimplerQMS

In Ideagen Quality Management, documents are Word or PDF files attached to the record.[^id-help-docs] In [SimplerQMS](/reviews/simplerqms/), documents are written in Word, Excel or PowerPoint and checked back in, and a Word add-in syncs document properties.[^sq-tech][^sq-help-word] It starts at $17,500 a year for up to 15 users, including implementation, IQ/OQ/PQ validation, data migration and training.[^sq-pricing] Its terms add a fixed 5% to all prices every 1 January, so renewal increases are known in advance.[^sq-terms] When a subscription ends, it exports all content as Excel metadata files plus the documents, at no extra charge.[^sq-terms][^sq-pricing] Customers can choose US or EU hosting.[^sq-qualio][^sq-help-region] It doesn't solve the design-control gap: design controls and risk are document collections rather than linked records.[^sq-design][^sq-risk] Contracts renew automatically with a 90-day notice period, and you need Microsoft 365 licences.[^sq-terms][^sq-tech]

### You make devices and drugs and want an easier system: Qualio

[Qualio](/reviews/qualio/) runs deviations, OOS and pharmacovigilance in the same platform as its device design controls.[^q-pharma] Those design controls support up to three requirement levels with verification and validation test cases and ISO 14971 risk.[^q-dc] G2 reviewers rate its ease of use 9.0/10, against 7.5/10 for Ideagen Quality Management (Sep 2026).[^q-g2][^id-g2] Its exit exports are documented: documents, training, events, suppliers and the audit trail, in PDF, Word, XLSX and CSV.[^q-security][^q-permissions] If you ask in writing before the end date, you get up to 30 days to retrieve your data.[^q-tos] Its web application is hosted on AWS in Dublin.[^q-subprocessors] Qualio doesn't publish prices, and every plan carries an implementation fee.[^q-pricing] We found no FDA MDR or EU vigilance reporting.[^q-qmsr]

### You're a very small team: OpenRegulatory Formwork

[Formwork](/reviews/formwork/) publishes flat prices: Starter costs 99 € a month plus VAT for up to 5 users, and QMS + Techdoc costs 499 € a month plus VAT for unlimited users.[^fw-pricing-live] Starter can't release product documentation, so a team heading for an audit needs the 499 € tier.[^fw-pricing-article] Requirements link to risk controls and tests, and each product records its IEC 62304 safety class.[^fw-swr][^fw-techdoc] It is weaker exactly where Ideagen is strong. Complaints are logged as incidents with no documented investigation step, and we found no internal audit planning; audit findings appear only as non-conformities.[^fw-incidents][^fw-nc] The vendor has no ISO 27001 certification and offers no audit rights.[^fw-audits] It has 2 reviews on G2, too few for a rating.[^fw-g2] Its terms of service describe yearly auto-renewal, which contradicts the "cancel any time" marketing.[^fw-tos]

## When to stay with Ideagen Quality Management

Ideagen Quality Management has real strengths, and switching an eQMS takes work:

- **Documented workflows.** The public help centre documents document control, CA/PA, complaints, suppliers, audits and training in detail.[^id-help-api]
- **Part 11.** A supplement covers Part 11 clause by clause, and administrators can switch on e-signatures for each approval, closure and acknowledgement step.[^id-help-part11][^id-help-esign]
- **A known price ceiling.** The FastStart pack costs "below £20,000 per year" with 15 licences, setup and two days of training.[^id-faststart] Its public list prices haven't risen recently: the January 2026 G-Cloud list cut the platform fee from £15,000 to £12,000.[^id-gcloud-price][^id-gcloud15]
- **UK or EEA hosting.** Data stays in the UK, the EEA or elsewhere as agreed in the order form, Ideagen holds ISO 27001:2022, and the data processing agreement is public.[^id-gcloud][^id-dpa][^id-certs]
- **Single sign-on.** SAML SSO works with Entra ID, Okta and PingOne.[^id-help-sso]
- **Combination products.** The life sciences pack adds out-of-specification investigations and GMP-style change control.[^id-faststart-ls]

If you stay, make sure the order form names an annual term rather than the agreement's 24-month default, and negotiate the auto-renewal, the exit export and a renewal cap.[^id-mssa]

[^id-faststart]: [Ideagen: FDA and ISO 13485-ready medical device quality management (FastStart)](https://www.ideagen.com/lp/demos/quality/fast-start-pricing-medical-devices). Vendor website, checked 1 Oct 2026.
[^id-help-api]: [Ideagen Quality Management help centre](https://iqm-pro.help.ideagen.com/hc/en-gb). Vendor documentation; we searched the titles and text of all 618 public help-centre articles, 4 Oct 2026.
[^id-help-risk]: [Ideagen Quality Management help: How to perform a risk assessment](https://iqm-pro.help.ideagen.com/hc/en-gb/articles/360020708299-How-to-Perform-a-Risk-Assessment). Vendor documentation, checked 1 Oct 2026.
[^id-mssa]: [Ideagen: Master Software and Services Agreement, UK v28](https://www.ideagen.com/dam/jcr:c5330e95-8a42-4f06-86ca-208a55dc5917/UK%20MSSA%20v.28.pdf). Vendor contract terms, updated 24 Aug 2026, checked 1 Oct 2026.
[^id-gcloud]: [Digital Marketplace: Ideagen Quality Management Professional (formerly Q-Pulse)](https://www.applytosupply.digitalmarketplace.service.gov.uk/g-cloud/services/567215567041443). UK G-Cloud 14 listing written by the vendor, checked 1 Oct 2026.
[^id-g2-hike-a]: [G2: Ideagen Quality Management review by an administrator, 5 Dec 2024](https://www.g2.com/products/ideagen-quality-management/reviews/ideagen-quality-management-review-10609213). Review site, read 4 Oct 2026.
[^id-g2-hike-b]: [G2: Ideagen Quality Management review by an administrator, 5 Aug 2025](https://www.g2.com/products/ideagen-quality-management/reviews/ideagen-quality-management-review-11492659). Review site, read 4 Oct 2026.
[^id-g2-hike-c]: [G2: Ideagen Quality Management review by an administrator, 2 Oct 2023](https://www.g2.com/products/ideagen-quality-management/reviews/ideagen-quality-management-review-8686732). Review site, read 4 Oct 2026.
[^id-capterra]: [Capterra: Ideagen Quality Management reviews](https://www.capterra.com/p/155354/Ideagen-Quality-Management/reviews/). Review site, checked 30 Sep and 1 Oct 2026.
[^id-gcloud-price]: [Ideagen Quality Management Professional pricing document, G-Cloud 14](https://assets.applytosupply.digitalmarketplace.service.gov.uk/g-cloud-14/documents/704432/567215567041443-pricing-document-2025-10-14-1221.pdf). Vendor price list, dated 14 Oct 2025, checked 1 Oct 2026.
[^id-g2]: [G2: Ideagen Quality Management reviews](https://www.g2.com/products/ideagen-quality-management/reviews). Review site, ratings checked 30 Sep 2026; review labels sampled and review texts read 4 Oct 2026.
[^gg-pricing]: [Greenlight Guru: Quality pricing and packages](https://www.greenlight.guru/quality-pricing). Vendor website, checked 29 Sep 2026.
[^gg-tour]: [Greenlight Guru: Interactive product tour](https://capture.navattic.com/clwik2336000209jseofsekzc). Vendor product tour with screenshots (captured 2024), checked 30 Sep 2026.
[^gg-pd]: [Greenlight Guru: Product development software](https://www.greenlight.guru/product-development-software). Vendor website, checked 29 Sep 2026.
[^gg-vendr]: [Vendr: Greenlight Guru pricing](https://www.vendr.com/marketplace/greenlight-guru). Price benchmark, checked 29 Sep 2026.
[^gg-msa]: [Greenlight Guru: Master subscription agreement](https://www.greenlight.guru/master-subscription-agreement). Vendor legal page, updated 26 Aug 2026, checked 1 Oct 2026.
[^gg-reddit-worth]: [r/MedicalDevices: Is Greenlight Guru worth using?](https://www.reddit.com/r/MedicalDevices/comments/1k05y0i/is_greenlight_guru_worth_using/). Community discussion, Apr 2025.
[^mx-trace]: [Matrix One user manual: Traceability](https://docs.matrixreq.com/en/articles/234192-traceability). Help center, checked 29 Sep 2026.
[^mx-git]: [Matrix One user manual: GitHub and GitLab integration](https://docs.matrixreq.com/en/articles/240976-github-and-gitlab-integration-with-matrix-requirements). Help center, checked 29 Sep 2026.
[^mx-sxmd]: [Matrix One blog: SxMD templates package](https://matrixone.health/blog/sxmd-templates-package). Vendor blog, published 2 Oct 2023.
[^mx-trial]: [Matrix One: Free trial](https://matrixone.health/trial). Vendor website, checked 29 Sep 2026.
[^mx-list2026]: [Matrix One: Company Plus plan page](https://matrixone.health/pricing/plans/company-plus). Vendor price page, updated Feb 2026, checked 29 Sep 2026.
[^mx-quality]: [Matrix One: Matrix Quality product page, ROI calculator and FAQ](https://matrixone.health/products/matrix-quality). Vendor website, checked 29 Sep 2026.
[^kx-dhf]: [Ketryx docs: How to generate the Design History File for your medical device (archived)](https://web.archive.org/web/20251015061057/https://docs.ketryx.com/how-to-guides/how-to-generate-the-design-history-file-for-your-medical-device). Product documentation, captured 15 Oct 2025.
[^kx-signup]: [Ketryx: Sign up for a free trial](https://app.ketryx.com/auth/signup). Vendor website, checked 30 Sep 2026.
[^kx-pricing]: [Ketryx: Pricing](https://www.ketryx.com/pricing). Vendor website, checked 4 Oct 2026.
[^kx-llms]: [Ketryx: AI-readable site index](https://llm.ketryx.com/llms.txt). Vendor website mirror (743 pages searched), checked 30 Sep 2026.
[^sq-tech]: [SimplerQMS: Technology platform](https://simplerqms.com/technology-platform/). Vendor website, checked 30 Sep 2026.
[^sq-help-word]: [SimplerQMS help: Using the SimplerQMS Word add-in](https://help.simplerqms.com/en/articles/12791795-using-the-simplerqms-word-add-in). Vendor documentation, checked 30 Sep 2026.
[^sq-pricing]: [SimplerQMS: Pricing and licenses](https://simplerqms.com/pricing/). Vendor website, checked 30 Sep 2026.
[^sq-terms]: [SimplerQMS A/S: Terms and conditions](https://simplerqms.com/terms-and-conditions/). Vendor legal page, last updated 14 Oct 2024, checked 30 Sep 2026.
[^sq-qualio]: [SimplerQMS: SimplerQMS vs Qualio](https://simplerqms.com/comparisons/qualio/). Vendor comparison page (used only for statements about SimplerQMS itself), checked 30 Sep 2026.
[^sq-help-region]: [SimplerQMS help: Consistent document numbering and process owner control](https://help.simplerqms.com/en/articles/14060523-ensure-consistent-document-numbering-process-owner-control). Vendor release notes, Mar 2026.
[^sq-design]: [SimplerQMS: Design control software](https://simplerqms.com/modules/design-control/). Vendor website, checked 30 Sep 2026.
[^sq-risk]: [SimplerQMS: Risk management](https://simplerqms.com/modules/risk-management/). Vendor website, checked 30 Sep 2026.
[^q-pharma]: [Qualio: Pharma quality management software](https://www.qualio.com/solutions/pharma-quality-management-software). Vendor website, checked 29 Sep 2026.
[^q-dc]: [Getting Started with Design Controls in Qualio](https://docs.qualio.com/en/articles/6596510-getting-started-with-design-controls-in-qualio). Vendor help center, checked 29 Sep 2026.
[^q-g2]: [Qualio reviews on G2](https://www.g2.com/products/qualio/reviews). Review site, checked 29 Sep 2026.
[^q-tos]: [Qualio: Terms of Service](https://www.qualio.com/docs/terms). Vendor legal page (effective 13 Aug 2024), checked 1 Oct 2026.
[^q-security]: [Qualio Security Practices](https://docs.qualio.com/en/articles/4071-qualio-security-practices). Vendor help center, checked 29 Sep 2026.
[^q-permissions]: [Qualio: User Permissions](https://docs.qualio.com/en/articles/6526420-user-permissions). Vendor help center, checked 29 Sep 2026.
[^q-subprocessors]: [Qualio: Terms and Policies (subprocessor list)](https://docs.qualio.com/en/articles/7042812-terms-and-policies). Vendor help center, 24 Nov 2025.
[^q-pricing]: [Qualio: Plans and pricing](https://www.qualio.com/pricing). Vendor website, checked 29 Sep 2026.
[^q-qmsr]: [Qualio's Content Pathway revision for FDA's new QMSR regulation](https://docs.qualio.com/en/articles/12888913-qualio-s-content-pathway-revision-for-fda-s-new-qmsr-regulation). Vendor help center, checked 29 Sep 2026.
[^fw-pricing-live]: [Formwork pricing, archived 3 Oct 2026](https://web.archive.org/web/20261003032601/https://openregulatory.com/pricing). Vendor website (Wayback Machine), read 4 Oct 2026; also checked in a browser 1 Oct 2026.
[^fw-pricing-article]: [Formwork eQMS pricing, and when you should upgrade, archived 21 May 2025](https://web.archive.org/web/20250521173444/https://openregulatory.com/formwork-eqms-pricing-and-when-you-should-upgrade/). Vendor documentation, updated 5 Mar 2025.
[^fw-swr]: [Software requirements and design inputs in Formwork, archived 25 Apr 2025](https://web.archive.org/web/20250425090838/https://openregulatory.com/software-requirements-and-design-inputs-in-formwork/). Vendor documentation, updated 1 Oct 2024.
[^fw-techdoc]: [Documenting your medical device in Formwork, archived 25 Apr 2025](https://web.archive.org/web/20250425091145/https://openregulatory.com/documenting-your-medical-device-in-formwork/). Vendor documentation, updated 1 Oct 2024.
[^fw-incidents]: [Formwork Manual: Incidents & Complaints, archived 4 Oct 2026](https://web.archive.org/web/20261004123314/https://openregulatory.com/formwork/manual/incidents-complaints). Vendor documentation, published 9 Sep 2026.
[^fw-nc]: [Formwork Manual: Non Conformities, archived 4 Oct 2026](https://web.archive.org/web/20261004123513/https://openregulatory.com/formwork/manual/non-conformities). Vendor documentation, published 9 Sep 2026.
[^fw-audits]: [Formwork Manual: Compliance & Passing Audits, archived 4 Oct 2026](https://web.archive.org/web/20261004123605/https://openregulatory.com/formwork/manual/compliance-and-passing-audits). Vendor documentation, published 22 Jan 2026.
[^fw-g2]: [G2: Formwork eQMS reviews](https://www.g2.com/products/formwork-eqms/reviews). Review site, checked 30 Sep 2026.
[^fw-tos]: [Formwork terms of service](https://app.openregulatory.com/terms_of_service). Vendor legal page, checked 4 Oct 2026.
[^id-help-part11]: [Ideagen Quality Management help: 21 CFR Part 11 Supplement](https://iqm-pro.help.ideagen.com/hc/en-gb/articles/19478545835794-21-CFR-Part-11-Supplement). Vendor documentation, updated 15 Dec 2025, checked 1 Oct 2026.
[^id-help-esign]: [Ideagen Quality Management help: Configuring electronic signatures](https://iqm-pro.help.ideagen.com/hc/en-gb/articles/360005741400-Configuring-electronic-signatures). Vendor documentation, updated 21 Jan 2026, checked 1 Oct 2026.
[^id-gcloud15]: [Ideagen Quality Management Professional pricing document, G-Cloud 15](https://assets.applytosupply.digitalmarketplace.service.gov.uk/g-cloud-15/documents/704432/307017188120620-pricing-document-2026-01-26-1145.pdf). Vendor price list, dated 26 Jan 2026, checked 1 Oct 2026.
[^id-dpa]: [Ideagen: Customer data processing agreement, revision 6](https://www.ideagen.com/dam/jcr:59703e3d-e390-48d4-bbb5-79509ef51936/ideagen-data-processing-agreement-rev6.pdf). Vendor legal document, updated 24 Feb 2026, checked 1 Oct 2026.
[^id-certs]: [Ideagen: Certifications and memberships](https://www.ideagen.com/company/esg/infosec-iso-certifications). Vendor website, checked 1 Oct 2026.
[^id-help-sso]: [Ideagen Quality Management help: Configuring Okta for Single Sign-On](https://iqm-pro.help.ideagen.com/hc/en-gb/articles/21039034746386--Example-Configuring-Okta-for-Single-Sign-On-SSO). Vendor documentation, checked 1 Oct 2026.
[^id-help-docs]: [Ideagen Quality Management help: Overview of the Document lifecycle](https://iqm-pro.help.ideagen.com/hc/en-gb/articles/8348132144402-Overview-of-the-Document-lifecycle). Vendor documentation, checked 1 Oct 2026.
[^id-faststart-ls]: [Ideagen: Quality management for Life Sciences (FastStart)](https://www.ideagen.com/lp/demos/quality/fast-start-pricing-life-sciences). Vendor website, checked 1 Oct 2026.


Why people switch from Ideagen Quality Management: Design controls, ISO 14971 risk files, vigilance reporting and IEC 62304 support aren't documented as product features, and the standard agreement defaults to 24 months with automatic renewal unless the order form says otherwise. Review: https://bestqmssoftware.com/reviews/ideagen-quality/

## Alternatives ranked by overall score

1. [OpenRegulatory Formwork](https://bestqmssoftware.com/reviews/formwork/): 7.8/10, $7k/yr. Best for: You're an early-stage device startup, especially one building software, and want a cheap, self-serve QMS with templates and linked requirements, risks and tests.
2. [Matrix Requirements (Matrix One)](https://bestqmssoftware.com/reviews/matrix-requirements/): 7.5/10, from $22k/yr. Best for: You build software or software-heavy devices and need design controls, risk and test traceability tied to your QMS.
3. [Greenlight Guru](https://bestqmssoftware.com/reviews/greenlight-guru/): 7.4/10, from $12k/yr. Best for: You build a medical device, want design controls, ISO 14971 risk and quality events linked in one MedTech-only system, and can budget well above the entry price.
4. [Cognidox](https://bestqmssoftware.com/reviews/cognidox/): 7.2/10, from $8k/yr. Best for: You run a small or mid-sized device company, want strong document control with Part 11 e-signatures at a low price, and are happy to shape your own CAPA, change and supplier forms.
5. [SimplerQMS](https://bestqmssoftware.com/reviews/simplerqms/): 7.1/10, from $17.5k/yr. Best for: You run a small or mid-sized device or pharma company, write your SOPs in Microsoft Word, and want implementation, validation and training included in one yearly price.
6. [Qualio](https://bestqmssoftware.com/reviews/qualio/): 6.8/10, est. $12–30k/yr. Best for: You're a growing device or combined device-and-pharma company that wants a QMS your whole team will actually use, with design controls linked to Jira and data hosted in the EU.
7. [Orcanos](https://bestqmssoftware.com/reviews/orcanos/): 6.7/10, pricing on request. Best for: You build a software-heavy or electromechanical device and want requirements, risk, tests and QMS records traced in one system rather than two tools joined by an integration.
8. [Arena QMS](https://bestqmssoftware.com/reviews/arena-qms/): 6.6/10, est. $12–25k/yr. Best for: You build physical medical devices with outsourced manufacturing and want CAPA, complaints, training and design records linked to the same BOM and change orders as your engineering data.
9. [Ketryx](https://bestqmssoftware.com/reviews/ketryx/): 6.5/10, pricing on request. Best for: You build software as a medical device, your engineers live in Jira and Git, and you want design controls, risk and IEC 62304 records generated from that work.
10. [Scilife](https://bestqmssoftware.com/reviews/scilife/): 6.3/10, pricing on request. Best for: You run a GMP-regulated pharma, biotech or combined device and pharma operation and want an easy-to-learn eQMS with validation documents included.
11. [Dot Compliance](https://bestqmssoftware.com/reviews/dot-compliance/): 5.9/10, pricing on request. Best for: You run a device, pharma or combination-product company and want a pre-configured GxP quality system on Salesforce that goes live in weeks to a few months.
12. [ETQ Reliance (Octave Reliance)](https://bestqmssoftware.com/reviews/etq-reliance/): 5.1/10, pricing on request. Best for: You run a multi-site medical device or combined device and pharma manufacturer and want one configurable system for documents, CAPA, complaints with eMDR, suppliers and audits across sites.
13. [MasterControl](https://bestqmssoftware.com/reviews/mastercontrol/): 5.1/10, est. $25–72k/yr. Best for: You run a larger, multi-site device or combined device-and-pharma quality organisation and need a configurable, validated system for documents, training, CAPA and audits.
14. [Qualityze](https://bestqmssoftware.com/reviews/qualityze/): 4.9/10, pricing on request. Best for: You make physical devices or combine devices and pharma, already use Salesforce or want to, and need configurable complaint, vigilance, CAPA and supplier workflows across several sites.