Top 10 Alternatives to H&A Healthcare Consulting Recently Reviewed By G2 Community
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Autodesk Forma (formerly Autodesk Construction Cloud) connects workflows, teams and data at every stage of construction to reduce risk, maximize efficiency, and increase profits. Built on a unified platform and common data environment, Autodesk Construction Cloud empowers general contractors, specialty trades, designers and owners to drive better business outcomes. Construction teams will have a comprehensive construction management platform with all data in one central location to simplify collaboration, proactively anticipate project changes and provide data-driven guidance for organizational improvement.
VelocityEHS is different. They're not just a software company, they're expert problem solvers who know how to simplify complex issues to deliver exceptional outcomes. Whether you’re a global enterprise or a smaller organization with big aspirations, a partnership with VelocityEHS provides your team with an approach to EHS & ESG that is smart enough to predict and address your challenges without overwhelming or adding unnecessary complexity. For more information, visit their website at https://www.ehs.com/solutions.
Autodesk PLM provides a central source of data that manages your processes and workflows. Connect your people, processes, and data with Autodesk PLM to get your products to market faster.
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.
Polygon One is the compliance software of HRG Polygon One GmbH, Düsseldorf, for the EU Deforestation Regulation (EUDR) and the EU packaging regulation (PPWR). Suppliers enter their plots through a portal without login, geolocation data is checked before import, and every plot is screened by satellite against 31 December 2020. The due diligence statement goes directly to TRACES, and the reference and verification numbers come back into the record. Platform data is stored with AWS in Frankfurt.
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.
flowise is a quality management software built for engineering consulting firms, IT services companies and technical assistance firms. Connected to the Boond ERP, it imports employees, assignments, clients, skills and assignment reviews every night and turns them into audit evidence. It covers ISO 9001, MASE, CEFRI, ISO 19443, ISO 27001, ISO 14001 and ISO 45001 in a single system: requirement-by-requirement compliance, action plans, nonconformities, internal audits, management reviews, KPIs, document control and certification tracking. Depending on the plan, it comes with a ready-written quality system for engineering consulting and support from a quality expert.
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.
SORQA ist die Web-App für Sortieranalysen im Abfall- und Recyclingbereich: Sortieranalysen, die sich von selbst dokumentieren. Wer Sortieranalysen macht, kennt das: Zettel in der Halle, Zahlen am Abend abtippen, Fotos in drei Chats, Rückfragen vom Auftraggeber. SORQA ersetzt das durch eine durchgehende digitale Dokumentation, direkt an der Probe, auf Handy oder Tablet. Was SORQA kann: • Erfassen: Mengen, Stückzahlen und Merkmale per Zahlenblock oder Diktat, jede Eingabe mit Zeit und Person • Wiegen: von Hand oder mit angeschlossener Waage, mit Foto • Foto-Belege: automatisch dem richtigen Eintrag zugeordnet • Soll und Ist: Ampelstatus je Auftrag, damit jeder sieht, was fertig ist und wo es hakt • Etiketten und QR-Codes direkt aus der App drucken • Schichtplan, Dispo und Kosten, die aus der echten Arbeitszeit lernen • Auch ohne Netz: Eingaben bleiben erhalten und werden nachgesendet • Export: alle Daten als Excel-Datei, auf Wunsch mit Fotos Prüffähig dokumentiert: Änderungsverlauf, Rollen und Freigaben, Foto-Belege. So lassen sich Rückfragen von Auftraggebern und Prüfern in Minuten beantworten. SORQA ist dafür gebaut, Nachweise sauber vorzubereiten, ist aber selbst nicht zertifiziert. Die App passt sich an: eigene Begriffe, eigene Abläufe, eigene Etiketten, eigene Auswertungen. Gehostet in Deutschland. Interesse an einer Vorführung? Schreiben Sie uns an info@sorqa.de oder besuchen Sie sorqa.de.