Medical Device RA & Quality Management Expert on the GPT Store
GPT Description
GPT Prompt Starters
- How to ensure compliance with EU MDR?
- Explain FDA requirements for medical devices.
- Define ISO 13485 standards.
- Components of a clinical evaluation report for MDR?
Medical Device RA & Quality Management Expert GPT FAQs
More custom GPTs by chen li on the GPT Store
Best Alternative GPTs to Medical Device RA & Quality Management Expert on GPTs Store
Medical Device Regulatory Advisor
Expert in EU/US med device regs, IVDR, ISO standards, MDR, FDA, with online referencing.
10K+
Medical Device QMS Assistant EU, USA & Pharmerging
An AI tool designed to support quality and project management teams in developing and maintaining a Legal Manufacturer Quality Management System that aim to comply with both USA and European regulations. This tool periodically improves to streamline processes. Last update: January 13th 2025
900+
Medical Device Consultant
Expert in medical device development and quality assurance, focusing on regulatory compliance.
600+
Medical Device Regulations Expert
Expert on EU Medical Device Regulations (MDR), In Vitro Medical Device Regulations (IVDR) & Medical Device Single Audit Program (MDSAP)
200+
医疗器械法规注册指南（NMPA)
提供专业的医疗器械法规注册咨询服务，并提供相关原始法规和注册指导文件的下载链接
200+
Medical Device Regulation (MDR) Advisor (EU)
with knowledge of ISO 13485 and ISO 14971
100+
Medical Device Regulation and Certification
Expert in medical device regulations and certification.
100+
Medical Device Sales Mastery
Elevate your medical device sales techniques and market acumen for a thriving career in this specialized industry. Gain an edge with tailored strategies that propel you to success. 💼📈
90+
Medical Device Engineering
A medical engineering assistant
80+
Medical Device News
Delivers latest updates on regulations, guidances and standards
60+
The EU Medical Devices Assistant
Delivers detailed responses about Quality and Regulatory Affairs (QA/RA) topics in Medical Devices domain.
50+
Medical Device Regulatory Assistant
Your International Medical Device Regulations Assistant
40+
Medical Device Safety Alerts
Get the latest Medical Device Safety Alerts globally
30+
Medical Device Advisor
Professional, approachable advisor in Medical Device Industry.
30+
BureauMed
Medical Device (include IVDs) Registration Pathway ● Clinical Study ● Technical Documentations Writing ● Report reviewing ● Classification ● Get Regulatory-based Answers and Accurate Citations.
30+
The USA Medical Devices Expert
Delivers detailed responses about Quality and Regulatory Affairs (QA/RA) topics in Medical Devices domain.
20+
Medical Device Classifier
Classifies medical devices based on MHRA rules.
20+
CyberMed Consultant
Cybersecurity consultant for Medical Devices, expert in MDR, FDA, and cybersecurity practices.
10+
Medical Device Development Mentor
Guiding in medical device development, focusing on industry standards and innovation.
10+
RA Advisor
Expert RA Advisor in global medical device regulations.
7+