
EU MDR GPT on the GPT Store
GPT Description
Welcome Message
GPT Prompt Starters
- What does Article 22 of EU MDR mean?
- How do I comply with EU MDR for a new device?
- Explain the post-market surveillance requirements in EU MDR.
- What are the labeling requirements under EU MDR?
EU MDR GPT FAQs
More custom GPTs by Dinesh Puppala on the GPT Store
CiteMaster
Guides users in creating accurate citations.
100+

VisaBot
I assist with visa requirements and processes.
80+

GiphMaker
Make Animated Giphs
20+

SpinGPT
High-volume article spinner with advanced paraphrasing AI
10+
WishGPT
AI for text and image-based personalized greetings and cards.
8+
QR Code Generator
QR Code Generator | Create Your Free QR Codes
1+

GuruGPT
Learn anything from Gurujipt
1+

Best Alternative GPTs to EU MDR GPT on GPTs Store
Eu Desenho
Transforma fotos em avatares com opções de personalização avançadas e feedback interativo.
100K+
Meta Prompt Lendário
Eu deixo seu prompt Lendário ♾️
50K+
Medical Device Regulatory Advisor
Expert in EU/US med device regs, IVDR, ISO standards, MDR, FDA, with online referencing.
10K+
Especialista em investimentos
Eu ofereço análises detalhadas de oportunidades de investimento, abrangendo desde ações e títulos até criptomoedas e imóveis, adaptadas ao seu perfil de risco e objetivos financeiros
10K+
Gestor de Tráfego - V4 Company
Eu vou te ajudar em tarefas essenciais, incluindo o planejamento e execução de campanhas de tráfego pago digital e análise de dados para atrair tráfego qualificado aos canais digitais empresariais, visando impulsionar conversões e crescimento.
1K+
ScholarAI em português
Eu pesquiso e analiso texto, figuras e tabelas em mais de 200 milhões de artigos e livros científicos para gerar novas hipóteses, e também navego pela internet em geral.
1K+
EU AI Act Insight
🇪🇺 Specialist in the EU Artificial Intelligence Act. ℹ️ Use any language. Ask "?" or "Help" for relevant questions. Full version of the agreement is here: https://www.kapler.cz/ai-act-dohoda/
1K+
EU MDR Product Classifier
Assistant for product classification according to EU MDR 2017/745.
400+
ADHOCON - Regulation SaMD & AI in Healthcare
Expert in EUMDR, US, IMDRF and EU AI Act
400+
EU MDR 2017/745
Ask anything about EU MDR
200+
MDR and IVDR Navigator
Conversational guide to EU MDR, IVDR, and MDCG guidance documents, with clear, bullet-pointed answers.
200+
Medical Device Regulations Expert
Expert on EU Medical Device Regulations (MDR), In Vitro Medical Device Regulations (IVDR) & Medical Device Single Audit Program (MDSAP)
200+
Medical Device Regulation (MDR) Advisor (EU)
with knowledge of ISO 13485 and ISO 14971
100+
MDR Advisor
Expert in EU medical devices registration, offering links to download regulation documents and guidances on MDR
100+
Medical Device Regulatory Assistant
Your International Medical Device Regulations Assistant
40+
MDReg
Guides on EU MDR compliance for medical device manufacturers.
20+
QA Specialist (Medical Devices - EU)
Expert in EU medical device QA processes. Trained on legal regulations (MDR, IVDR, GDPR, REACH, RoHS, WEEE). Disclaimer: Every AI can make mistakes
20+
MDR Navigator
Guides on AI healthcare device compliance with EU MDR, using uploaded documents.
10+
MDR-o
MDR legal expert, focusing on EU MDR, specific to Spain on request
10+
MDR Guide
Expert on EU Medical Device Regulation, offering information and guidance.
7+