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CertHub is an AI-driven platform designed to streamline compliance and regulatory processes for medical device manufacturers. By automating tasks associated with the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), CertHub enables companies to focus on innovation without being hindered by complex paperwork. Key Features and Functionality: - Fast Track to Certification and QMS ISO 13485: CertHub's AI Certification Assistant prepares Quality Management Systems (QMS) and technical documentation for submission within weeks, ensuring accuracy and alignment with specific medical devices. - 1-Click Documentation - eTD and eQMS: The platform offers fully validated electronic Technical Documentation (eTD) and electronic Quality Management Systems (eQMS), making documentation audit-ready with a single click, whether starting anew or integrating existing files. - Clinical Research Agent: CertHub provides a plug-and-play AI agent that manages the entire clinical evaluation process, from search strategy to full-text analysis, without requiring integration. - AI Conformity & Gap Checker: The platform assesses documentation readiness from inception to submission, performing gap analyses and pre-audit checks to ensure each entry is defensible. Primary Value and Solutions for Users: CertHub addresses several challenges faced by medical device manufacturers: - Automated Compliance Workflows: By automating regulatory tasks, CertHub reduces manual work and errors, streamlining the compliance process. - Integrated Submissions: The platform offers one-click solutions for MDR and FDA submissions, simplifying complex procedures and saving time. - Real-Time Monitoring: CertHub provides proactive compliance checks and alerts, helping companies stay ahead of regulatory requirements. - Centralized Documentation: All regulatory and quality documents are stored in one place, facilitating easy access and audit readiness. - Global Regulatory Alignment: Supporting multiple standards, CertHub enables seamless expansion into new regions by aligning with various regulatory frameworks. By leveraging CertHub, medical device manufacturers can cut compliance costs by 30%, accelerate time-to-market by 40%, and reduce product recalls by 50% through continuous compliance monitoring and proactive risk management.
Open CPD helps training providers issue branded CPD certificates and digital badges to learners, one at a time or in bulk from a spreadsheet. Every certificate has a unique verification ID and a permanent public achievement page, so learners can share it and employers can check it online. You set up your organisation profile and course profiles once, then issue certificates for each course or event, individually or in bulk by uploading a CSV file. Each learner receives a branded CPD certificate and an Open Badge digital badge, both with a unique verification ID. Each certificate also has its own persistent, public achievement page showing the course details, learning outcomes, skills and provider profile. Learners can share these on LinkedIn, in a CV or in an email signature, and employers can verify them in seconds. Certificates are stored so they cannot be altered after issue. You can choose from over 20 professional templates, add partner or client logos, issue in multiple languages, and award your own CPD points. Course profiles are free to create and reuse, and you only use credits when you issue a certificate. You can start on pay-as-you-go and move to a subscription once your volume justifies it. Open CPD does not accredit or endorse training. The credibility comes from the provider publishing their own training, under their own name, on an independent platform. Open CPD certificates are powered by Open CPD, and the training stays yours. Open CPD is built for small and medium-sized training providers, consultants who deliver training, professional bodies, charities and conference or event organisers. You can go from sign-up to your first certificate in a day. It works with any LMS through CSV upload, Zapier or Zoho Flow, and an API is available for high-volume use. It is used by about 200 training providers in more than 30 countries.
MedDeviceAudit is an AI-powered compliance auditing platform built specifically for medical device manufacturers. It audits technical files against FDA QMSR 2026 (21 CFR Part 820), ISO 13485:2016, IEC 62304, and ISO 14971 — returning evidence-anchored findings grounded in your actual documents with SHA-256 verified citations, literal quotes, and page references. Every finding is mapped to the exact regulatory clause it evaluates. Zero-retention data policy — uploaded documents are permanently deleted after every audit. No document is ever stored, shared, or used to train AI. First audit always free with no credit card required. Plans from $495 per month for 5 document audits per month. Works for Class I, II, and III medical devices including SaMD.
NittyHSEPro helps small and mid-sized contractors in rail, construction, civil engineering, manufacturing, logistics and energy keep health, safety, quality and environmental records in one place. Teams capture inspections, close calls, risk assessments, permits to work and training records on site from their phones, and managers export branded PDF evidence packs for client, Tier 1 and RISQS audits. It includes ISO 45001, 14001 and 9001 clause-level gap analysis, AI-drafted RAMS and templates, contractor pre-qualification, e-learning, and ESG/carbon tracking. Built by Abdulwaheed Oluwasegun, IRCA Lead Auditor and CertIOSH. Data stored in the EU (Ireland).
Traffic management plan software made in New Zealand. Xuro Designer is for drawing TMPs on real NZ aerials. The Xuro Review Engine checks a finished TMP package before you submit it. Draw traffic management plans on real NZ aerials, then check the whole package against CoPTTM or NZGTTM before you submit. NZ signs from NZTA’s own sign files, Austroads AP-G34-23 design vehicles for swept paths, and uploaded PDFs deleted after 30 days. Runs in Chrome or Edge. The Xuro Review Engine assists a qualified reviewer. It does not replace one, and it does not approve plans.
ISOauditor.app is an AI-powered audit assistant and training platform built specifically for ISO lead auditors and certification bodies. The audit assistant scribes and summarises interviews with key personnel in real time, processes documents and audio across multiple formats and 50+ languages, classifies evidence against the relevant ISO clauses, identifies gaps, suggests follow-up questions, and generates accurate, well-written audit reports. Every output is reviewed and approved by the auditor. Developed by ISO lead auditors and technology consultants, trained on thousands of hours of real-world audit data. The training suite pairs clause-by-clause standard knowledge with realistic AI companies to audit each with its own management system, documentation, and a fully responsive AI quality manager trained to behave like a real person. Auditors can practise finding hidden nonconformities, questioning technique, and report writing in complete safety. Available for ISO 9001, 14001, 27001 and 45001, with further standards being added.
foraudits collects, reads and checks every document against the standard. You keep the part that matters: the judgement, the decision, the signature.
Reg Review is an AI-powered compliance platform built for registered investment advisers (RIAs), private fund managers, exempt reporting advisers (ERAs), and broker-dealers, with versions available for insurance, real estate, and private credit firms. It helps compliance teams run their whole program in one place: annual reviews, mock exams, Form ADV and U4 disclosures, marketing reviews, vendor due diligence, registration tracking, and FinCEN AML readiness. Its Disclosure Center drafts filings like Form ADV Item 9, U4 DRPs, Reg S-P, cybersecurity, conflicts, and fee disclosures, with citations and deadline tracking built in. Reg Review was developed alongside FIN Group’s active consulting practice and refined by real CCOs doing live compliance work during beta. Tiered pricing scales from solo practitioners to enterprise firms.
Controvisto is the AI-use register with a "verified by a person" seal for professionals and firms. Record every use of AI in your work, state what a person actually checked (citations, legal references, client data), and seal the final PDF with a QR code that anyone can verify online: valid, revoked, or altered. Built for Italian Law 132/2025 (art. 13), which requires professionals to tell clients when and how AI was used. For lawyers, accountants, labour consultants, notaries, engineers, safety and privacy consultants, psychologists and journalists. Data hosted in the EU, two-step verification, trusted timestamps, encrypted backups. Plans from €9/month + VAT; firm plan for up to 5 people.
SegnalaChi is a cloud whistleblowing platform by One AM (ISO 9001 and ISO/IEC 27001 certified), compliant with Italian Legislative Decree 24/2023 and EU Directive 2019/1937, for public bodies, companies with 50+ employees, Model 231 entities and groups. Reporters submit anonymous written or voice reports without registering: voices are altered and attachment metadata is stripped automatically. A unique code lets them check the status and chat confidentially with the case handler, disclosing their identity only on request. Handlers get a dashboard with the legal 7-day and 3-month deadlines, roles for admins, internal and external operators (e.g. the Supervisory Body), private notes, an exportable audit log and email alerts without report content. Custom domain and logo, policy documents and privacy notice, multi-company management, reporting page in Italian, English and German. Report data encrypted with XChaCha20-Poly1305, hosted in Italy (Aruba datacenter, Bergamo) with encrypted daily backups in Bergamo and Rome, annual penetration test, 99.5% SLA, two-factor authentication, GDPR art. 28 processor. EUR 49 + VAT per month billed annually for any number of employees, no activation fees, 7-day free trial.