Amazon now requires ophthalmic drug product sellers to verify that they meet new policy requirements via third-party testing on an annual basis. NSF can help complete this verification – to get started, visit this Amazon Seller page: https://amzn.to/3CFxUGf
NSF - Life Sciences
商务咨询服务
Ann Arbor,Michigan 15,467 位关注者
NSF provides world-class consulting, training, clinical, and auditing services to the life sciences industry
关于我们
NSF works with pharmaceutical, medical devices, and in vitro diagnostic companies, large and small, to provide highly customized end-to-end services throughout the product lifecycle, from clinical trials to post-market surveillance. We are a global provider of clinical trials, training, consultancy, certification and auditing services to the life sciences industry. We have an outstanding international reputation in quality management and regulatory compliance. We provide comprehensive solutions for the life sciences industry from experts you can trust. Our team includes former FDA, EU and MHRA regulators as well as industry experts. We combine regulatory knowledge with industry best practices to provide our clients with tailored quality, compliance and regulatory services About NSF For 80 years our mission has remained the same: protect and improve human health. Our Values Building a healthy culture and looking after our people is fundamental to achieving our mission—and underpinning everything we do. Everything, not least client focus and growth, is built upon this. Our culture starts with four core values: Do the Right Thing; Treat People Well, Relentlessly Pursue Excellence, and We Are One NSF. These core values are the principles that guide all of NSF’s actions. Work at NSF - careers - https://www.nsf.org/about-nsf/careers
- 网站
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https://www.nsf.org/life-sciences
NSF - Life Sciences的外部链接
- 所属行业
- 商务咨询服务
- 规模
- 5,001-10,000 人
- 总部
- Ann Arbor,Michigan
- 类型
- 非营利机构
- 创立
- 1944
- 领域
- Clinical Trials、Product Lifecycle Support、Regulatory Strategy、Market Access、Regulatory Compliance Consulting、QMS Improvement、GMP Certification、Product and Ingredient Certification、Auditing and Inspections、Training and Education、Corporate Due Diligence、Remediation、Leadership Development and Coaching、Facilities, Equipment and Technical Support和Post-Market Surveillance
地点
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主要
789 N Dixboro Rd
US,Michigan,Ann Arbor,48105
NSF - Life Sciences员工
动态
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Tired of Packaging Recalls? Master Pharmaceutical Packaging Best Practices. Pharmaceutical packaging errors are a leading cause of recalls. Don't let this happen to your company. Our intensive 4-day training program equips you with the knowledge and skills to prevent costly mistakes and ensure patient safety. Learn about GMP, PQS, supply chain management, and more. Register now and transform your packaging processes! Visit at : https://bit.ly/3CNU9Kj
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Need to complete your 2024 training? Our Black Friday sale starts on November 18. For a limited time, get 50% off On-Demand, Self-Paced Life Sciences courses with promo code BLACKFRIDAY50 . Don’t miss out on this chance to prepare for the upcoming year. Please visit at: https://bit.ly/4fEWfuH
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Medical Device supplier non-compliance can compromise your entire operation. We help manufacturers conduct supplier audits and manage corrective actions to pinpoint and resolve vulnerabilities in your supply chain, protecting your product safety, compliance, and reputation. Learn more about how NSF can help ensure supplier compliance https://bit.ly/3VbjRyD
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Companies with low quality management maturity (QMM) exhibit certain tell-tale traits? What are they? NSF's Dr. Samantha Atkinson outlines them in the video below. Want to know more? Get the Quality Culture whitepaper, here: https://bit.ly/4iihZyf
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Master Equipment Qualification & Validation: Elevate Your Expertise!This comprehensive training from NSF International equips you with the skills to confidently navigate the complexities of equipment qualification and validation. Ensure compliance and boost efficiency in your operations. Learn more and register today: https://bit.ly/491lS6e
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The FDA’s new regulations for LDTs are fast approaching, with strict deadlines that could impact your laboratory’s operations if not met. This webinar offers detailed guidance to help you understand these new rules and implement necessary changes efficiently. STAGE 1 (Effective May 6, 2025): Focuses on establishing foundational compliance with Medical Device Reporting (MDR), correction, and removal reporting, and managing complaint files. Our industry experts, who conduct this webinar, have first-hand experience helping laboratories prepare and comply with the new regulations. Register Today! https://bit.ly/3CzQiQQ Can't make the date? We'll send a watch on-demand link.
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Avoid Costly FDA & FTC Violations: Dietary Supplement Claims Substantiation Training Don't let inaccurate claims jeopardise your brand. Our training equips you with the knowledge to ensure your dietary supplement labelling is fully compliant with FDA and FTC regulations. Learn to build strong substantiation, avoid implied claims, and understand the latest enforcement trends. Protect your business and your reputation. Register Now! https://bit.ly/40XQF1W
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A well-structured CAPA system is crucial for compliance and operational excellence. Yet, many organizations struggle with overly complex processes that can lead to delays and confusion. In our recent article, we discuss the advantages of a streamlined CAPA system and provide actionable insights to enhance its effectiveness in your organization.
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Did you know that over 50% of medical device compliance issues are discovered during external audits, often after internal teams have signed off on them? Internal teams can miss compliance gaps simply because they’re too close to the operations. Supplier audits carry even more risk, as any weak link in your supply chain can lead to non-compliance, delayed approvals, or product recalls. At NSF, our external audits provide a fresh, independent perspective that helps medical device companies identify risks early—before regulators do. Let’s talk about how outsourcing your internal and supplier audits can uncover risks before they become costly problems. https://bit.ly/3Z1eanV