Critical analyst of FDA practices, uncovering conflicts and scrutinizing data.
Rate: 4,1 ★
안녕하세요! 한국어 법률 KLB (Korean Legal Bot)입니다🥰 # Law # legal 데이터를 바탕으로 유용한 법률 정보를 제공할 수는 있지만, 심각한 법률 문제의 경우 전문 변호사와 상담하는 것이 항상 현명합니다. 또한, 저는 AI 챗봇으로 틀린 내용을 이야기 할 수 있으며, 어떠한 법률적 책임도 지지 않음을 알려드립니다. 💌소개 내용💌 (https://tilnote.io/pages/654f0dae02bfdae455cb4fd8)
Rate: 4,3 ★
Pharma Regulatory Expert- FDA, EMA, NMPA, WHO, ISPE, PICS, ICH
Rate: 4,4 ★
Expert in EU/US med device regs, IVDR, ISO standards, MDR, FDA, with online referencing.
Rate: 4,2 ★
Approachable expert on FDA medical device regulation. Offering direct download links for related regulation and guidance documents from FDA sites.
Rate: 4,2 ★
⭐️AP All-In-One: 🔬Integrate guidelines (WHO 5th, AJCC V9, ICD11...) 🌐Supported by academic databases (PubMed, FDA, USPTO...) & search engines (Google...) 📝Summarize path YouTube & notes 📊Data analysis via Python, R 🚀Its powerful capabilities can assist you with any path inquiries
Rate: 4,8 ★
An in-depth tool to discuss the policy proposals presented in the Project 2025 Mandate for Leadership.
Rate: 1 ★
Schedule a web observation watchdog that works even while you sleep
Rate: 4,3 ★
Validation Engineer / Quality Assurance / FDA Expert for Phamaceutical industries
Rate: 4,2 ★
I can support you in checking Food & Drugs Agency regulations for Pharmaceutical products sale in the USA I have access to over a hundreds FDA documents to double check my answers before providiing them. My Focus is on Manufacturing and Distribution
Rate: 5 ★
The cGMP Quick Reference of FDA Pharmaceutical Guides is a quick reference for published FDA guidance for the pharmaceutical manufacturing and pharmacy compounding industries in order to promote manufacturing quality. The guide can be multilingual for top 10 languages.
Rate: 5 ★
Insights into FDA drug regulations based on 1000+ latest guidance documents. Access to original documents for further reference will be available through provided download links.
Rate: 0 ★
Biotech QA & Compliance Expert with deep knowledge of FDA CFRs, ICH guidelines.
Rate: 0 ★
Factual information on all drugs: FDA approved, in clinical development, natural herbs, supplements , recreational/street substances.
Rate: 5 ★
Regulatory expert in FDA and ISO 13485, guiding on medical devices in the USA
Rate: 2,5 ★
Expert on FDA regulations for new drug development, clinical trial, manufacturing and marketing in the US