At DocuRegs, we've been busy since the holidays and still going, preparing and creating insightful information for you. Our goal is to help you start 2024 armed with knowledge in MedTech regulatory, quality, and engineering. We've recently launched a YouTube channel featuring video content on, #PMCF #FDA predicate devices and classification #ISO13485 development #SupplierManagement #RiskAssessment #Vigilance, and more! ????????Please visit our channel, subscribe, share, and like to stay informed. ???????????????? ??-?????????? ???????????? ???????? ?????????????? ????????: ??"????????????????: ???????????????????? ???????????????????? ?????? ?????????????? ???????????? & ???????????????????? ??????????????????????????." Co-Authors: Mike B. Wetherington and Leonard (Leo) Eisner Eisner, "The IEC60601 Guy." ??"???????????????????? ?????? ?????????? ?????????????? ???????????? ???????????????????? ??????????????????: ?? ?????????? ?????? ???????????????????? ?????????????? ??????????????????????????." Co-Authors: Mike B. Wetherington and Adam Isaacs Rae. ??"???????????????????? ?????? #SaMD ???????????????????? ????????: ?? ?????????????????????????? ?????????? ?????? ???????????????????? ?????????????? ??????????????????????????." Co-Authors: Mike B. Wetherington and Karandeep Singh Badwal. ??"Navigating the LATAM Regulatory Landscape: ?? ?????????????????????????? ?????????? ?????? ???????????????????? ?????????????? ??????????????????????????." Co-Authors: Mike B. Wetherington and Rishi Dewan MPharm, MSc, MTOPRA. At DocuRegs, our focus is on collaboration and contribution for the benefit of the community. If you have valuable insights on specific areas in #MedTech regulatory, quality, and engineering, we would love to hear from you. DocuRegs "???????????????? ????????????????????, ??????????????, ?????? ??????????????????????." ?? ??????-???????????? ??????????????????????. https://lnkd.in/gBK4ZzVW
DocuRegs
商务咨询服务
Navigating MedTech Success: Bridging Regulatory, Quality, and Engineering with Expert Tools and Insightful E-books.
关于我们
Welcome to DocuRegs LinkedIn Page! (Sister company of MedicalRegs) ?? Elevating MedTech Excellence ?? At DocuRegs, we're your dedicated partners on the journey to MedTech success. With a focus on Regulatory Affairs (RA), Quality Assurance (QA), and Medical Engineering, we're here to empower innovators like you with the tools, knowledge, and insights needed to thrive in the ever-evolving world of medical devices. ?? Your Trusted Guides: Our team of seasoned experts brings a wealth of experience across the MedTech spectrum. From deciphering complex regulatory landscapes to crafting innovative quality solutions and engineering advancements, we're here to guide you every step of the way. ?? Expertise in Your Hands: As advocates of continuous learning, we've curated a library of e-books that provide comprehensive guidance on medical device regulatory pathways, quality assurance best practices, and medical engineering standards. Dive into our resources to stay ahead of the curve. ?? Crafting Excellence: We believe that excellence isn't just a goal; it's a way of doing things. Our RA/QA tools are meticulously designed to streamline processes, enhance compliance, and fuel your growth. Because your success is our success. ?? Igniting Innovation: In the dynamic MedTech landscape, innovation is the driving force. Through our e-books and resources, we inspire creative thinking and bridge the gap between regulatory, quality, and engineering realms, ensuring your ideas come to life. Join us on this exhilarating journey of MedTech innovation and advancement. Follow our page to access valuable insights, stay updated on industry trends, and be a part of a community that's committed to shaping the future of healthcare. Let's navigate the path to MedTech success together! ??
- 网站
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DocuRegs.com
DocuRegs的外部链接
- 所属行业
- 商务咨询服务
- 规模
- 2-10 人
- 总部
- Jacksonville
- 类型
- 自有
- 创立
- 2023
- 领域
- Medical Device Regulatory Compliance、ISO13485、ISO14971、Risk Management、IEC60601、ASEAN Regulatory、Quality Management System、FDA 510k、CMDR、Home Healthcare Devices、Robotics、CAPA、PMS、PMCF、Clinical、Risk Assessment、Technical Documentation File、Product Safety、CB Scheme、Risk Mitigation、Risk Control、EU MDR、510k、Health Canada、QMS、Supplier Evaluation和Product Safety Certification
地点
动态
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DocuRegs转发了
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