AIMEDIQ, the AI-powered regulatory intelligence platform for clarity in MedTech, Pharma, and Biotech compliance
AIMEDIQ delivers fast, structured access to over 2,000 official regulatory documents across global markets, giving regulatory teams the intelligence they need to stay compliant, audit-ready, and ahead of regulatory change, from their first submission to their thousandth active registration.
PLATFORM SOLUTION
AIMEDIQ centralises regulatory intelligence, reduces manual workload, and keeps every answer traceable to its source
Swiss-engineered and AI-powered by DocDive from G+D Netcetera, AIMEDIQ simplifies how MedTech professionals manage regulatory standards. It delivers fast, structured access to essential regulatory information, all in one place and always up to date.
AIMEDIQ centralises over 2,000 official regulatory documents across global markets, delivers tailored AI responses based on your specific content and queries, and keeps every answer traceable to its original source — giving regulatory teams of every size the clarity and control they need to stay compliant and audit-ready.
WHY AIMEDIQ
Covering global market jurisdictions
Secure, centralised platform, powered by AI
Secure, closed AWS infrastructure in Frankfurt, Germany with tailored results based on your input
2,000+ official regulatory documents
Official regulatory documents spanning laws, directives, and guidelines across global markets
Submit your regulatory query in plain language
AIMEDIQ retrieves structured, relevant answers from its controlled regulatory knowledge base. No manual searching, no cross-referencing across multiple sources, no approximation.
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Receive structured, source-referenced answers tailored to your regulatory context
AIMEDIQ adapts to your specific content and regulatory context, delivering answers relevant to your device, your markets, and your compliance situation. Every response is directly linked to its original regulatory document, providing the full transparency and audit trail your team needs.
Continuously updated, always audit-ready, and ahead of regulatory change
AIMEDIQ continuously updates its document library from trusted official sources, monitors document validity across your portfolio, and alerts your team before standards expire, keeping your organisation compliant, current, and ahead of regulatory change at all times.
HOW AIMEDIQ WORKS
AIMEDIQ INDUSTRIES
Covering the full spectrum of Life Sciences, at any stage of growth
Regulatory complexity does not scale with company size. A startup preparing its first technical documentation package faces the same regulatory environment and the same compliance risks as a global MedTech leader managing thousands of active registrations.
AIMEDIQ serves medical device manufacturers, IVD manufacturers, pharmaceutical companies, biotech organisations, SaMD developers, regulatory affairs consultancies, and quality management teams across global markets. Organisations can also upload their own internal directives, SOPs, and licensed standards alongside the existing document library.
Medical Devices
From Class I to Class III, AIMEDIQ covers the full regulatory landscape for medical device manufacturers across every major global market.
In Vitro Diagnostics
Structured access to the regulatory frameworks governing IVD classification, performance evaluation, and market registration.
Software and Digital Health
Navigating the regulatory requirements for software-driven devices, health applications, and AI-enabled diagnostics across global markets.
Quality Management
Everything your quality management team needs to maintain audit-ready systems, in one centralised and always-updated platform.
AIMEDIQ KEY FEATURES
Full document traceability
Full transparency of sources across every response, so your team can focus on product development rather than regulatory administration.
Tailored results with complete visibility
AI adapts to your content for relevant, structured answers, all relevant documents linked, even with vague queries.
Custom uploads & unlimited access
Upload and manage your licensed standards alongside the existing library, with a flat-rate licence and no query limits.
Secure & Scalable
Closed AWS infrastructure in Frankfurt, Germany, scalable from agile startups to global MedTech leaders.
Smart alerts & expiry monitoring
Timely notifications before documents expire, reducing manual workload and keeping your team on top of regulatory change.
Real-time updates
Continuous updates from trusted regulatory sources covering regulatory changes and customer-specific standards, so your team is always ahead.