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Legal & RegulatoryEvent: September 7, 2026

ADHOCON notes that the FDA has a discussion paper and a pilot project named TEMPO for generative-AI medical devices.

Published

Signal category

Legal & Regulatory

Quote

The FDA has a discussion paper and a pilot - TEMPO - for exactly these generative-AI devices.

Rudolf Wagner|ADHOCON team

Company

ADHOCON

AI Enablement for Regulated Industries | On-Premise Agents | Open Source Tools | github.com/rlwadh

Industry
Business Consulting and Services
Location
Ludwigshafen am Rhein, DE
Company size
1 employees

ADHOCON helps regulated companies activate AI on their own infrastructure. No new tools. No SaaS. No data leaving your environment. We provide: → On-premise AI agent setup (Azure, AWS, Google Cloud) → Regulatory AI training & configuration → Open-source tools for regulatory intelligence Our open-source toolkit (github.com/rlwadh): → ReguWatch – Daily regulatory website monitoring (FDA, MDCG, IEC, ISO) → Regulatory Prompt Library – 10,000+ validated prompts for MedTech, Pharma, AI → FDA Predicate Finder – Live 510(k) search with openFDA API → MarkItDown – Document-to-Markdown Adhoc online services With our ADHOCON database sourced from over 150 Audits (as Auditor and Auditee) we are able to provide you the best practices and experience of Notified Body, Authority and Industry interactions. QA & Regulatory - full usable QMS-on-demand implemented incl. training within 1 week (cGMP, ISO13485 & 9001. EU MDR, EUDRALEX, US 21CFR, MDSAP), audit preparation, CAPA, deviation, complaint, backlog reduction, Authority communication, worldwide MedDev registration, Lean6S QMS improvement, mock-up recall, mock-up unannounced audit, Risk Management acc. ISO14971 We are in addition EUDAMED registered Authorized Representative for EU and PRRC. Small businesses can book our PRRC service and non-EU medical device manufacturers our AR & PRRC combination service Special Services Penetration testing - social engineering Regulatory departments hold all IP protected documentation or all errors ever happened. Competitors seek to steal them. We test your departments for those attacks and train them on preventive measures. Expert Witness and Appraisals As registered Expert Witness we investigate and write appraisals for courts for all classes Medical Devices and IVDs. C-Suite support We offer M&A due dilligence (Regulatory) for pharma and Medical Devices and offer QA & RA Forensics on persons, products and companies Business Contingency Management acc. ISO22301 - be ready for ANY crisis

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