Navigating through the sea of QMSR posts? Changes in regulations always drive the webinars and website postings. If you're simply looking for a summary that you can use to gather your thoughts for an organizational briefing, or assessment, try ours!! Note, I just sat in a webinar myself on the topic of risk in the QMSR by Greenlight Guru that was very well done. We're arming ourselves with pre-aligned Notified Body and engineering relationships for the wave that will be coming! #QMSR, #RAPS, #Ropes & Gray #SGS
关于我们
We are a small, Client-focused group of skilled medical device professionals offering regulatory services (RaaS). Our Clients receive tailored, risk-based solutions to meet their individual needs. med-sherpa offers experts in the fields of quality, regulatory, clinical affairs, and project management. We offer turn-key solutions through our subject matter expertise & strategy augmented with project management, and individual contribution. While we specialize in US and EU medical device compliance we can also offer support for other major market regulation sets like Canada, Japan, and Australia.
- 网站
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https://www.med-sherpa.com
med-sherpa, Inc. 的外部链接
- 所属行业
- 医疗设备
- 规模
- 2-10 人
- 总部
- Nashua，NH
- 类型
- 私人持股
- 创立
- 2020
- 领域
- MDR、ISO 13485、ISO 14971、Compliance、Medical Device、Quality、Regulatory、CAPA、QMS、RaaS、Regulatory as a Service、Risk Management、Post Market, Surveillance、Supplier Controls、Clinical Evaluation、Grace Period、Medical Devices Bill 2019-21、UKMDR、21CFR和MHRA
地点
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主要
获取路线
US，NH，Nashua
med-sherpa, Inc. 员工
动态
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Attention Medical Device Manufacturers! Do you need an Excel file listing all the MDCG docs issued from formation through Dec 2023 regarding the EU MDR? Look no further! Our team at Med-Sherpa has scraped all the info from the single source of truth, the EC website. This file could be a great basis for a compliance matrix or a reference guide. And the best part? We're offering it to you completely free of charge, no strings attached. Send us an email at [email protected] and we'll send you the file. #MedicalDeviceRegulations #EUMDR #ComplianceMatrix #ReferenceGuide #med-sherpa