Medical Device Regulatory Assistant on the GPT Store
GPT Description
GPT Prompt Starters
- How register a new medical device with the FDA?
- What is EUMDR?
- Compare medical device regulations
- Tell me more about MDSAP?
Medical Device Regulatory Assistant GPT FAQs
More custom GPTs by W&W on the GPT Store
Best Alternative GPTs to Medical Device Regulatory Assistant on GPTs Store
Medical Device Regulatory Advisor
Expert in EU/US med device regs, IVDR, ISO standards, MDR, FDA, with online referencing.
1K+
Medical Device Consultant
Expert in medical device development and quality assurance, focusing on regulatory compliance.
200+
Medical Device Regulation and Certification
Expert in medical device regulations and certification.
100+
Medical Device QMS Assistant
A cutting-edge AI tool designed to support quality assurance and project management teams in developing and maintaining a Legal Manufacturer Quality Management System that complies with both U.S. and European regulations. This tool focuses on continuous improvement to streamline QMS processes
100+
Regulatory Guide
Expert on FDA medical device regulations
60+
The EU Medical Devices Assistant
Delivers detailed responses about Quality and Regulatory Affairs (QA/RA) topics in Medical Devices domain.
50+
Medical Device News
Delivers latest updates on regulations, guidances and standards
50+
MDR Medical Device Classifier
Suggests the correct MDR classification for your medical device based on the MDR Annex VIII Classification Rules. Please provide a description of your device to get started. Note: Please always check recommendation with a qualified regulatory expert.
30+
Quality Assurance & Regulatory Affairs AI
Highly specialized in medical device regulations, generating detailed documents and reports.
30+
FDA Regulatory Support
Regulatory expert in FDA and ISO 13485, guiding on medical devices in the USA
30+
Medical Device Regulations Expert
Expert on EU Medical Device Regulations (MDR), In Vitro Medical Device Regulations (IVDR) & Medical Device Single Audit Program (MDSAP)
30+
Medical Device Advisor
Professional, approachable advisor in Medical Device Industry.
30+
The USA Medical Devices Expert
Delivers detailed responses about Quality and Regulatory Affairs (QA/RA) topics in Medical Devices domain.
20+
Regulatory Intelligence
Medical Device Regulation Expert with CSV List Output
10+
BureauMed
Medical Device (include IVDs) Registration Pathway ● Clinical Study ● Technical Documentations Writing ● Report reviewing ● Classification ● Get Regulatory-based Answers and Accurate Citations.
10+
中華民國醫療器材管理法專家
Expert on Taiwan's Medical Device Management Act, providing detailed regulatory info.
10+
Global Med Device Regulator
Global expert in medical device regulations
6+
Knowledge Base for Medical Device Regulatory
3+
Ceriter Report Specialist
Regulatory and market analysis expert for French medical device sector
2+
Medical Technology Consultant
Expert in integrating medical devices and IT systems into healthcare practices, ensuring regulatory compliance, data security, and enhanced patient care. | Made with ♥ by MyExperts.Solutions |