Work with our team of former regulators and industry experts to audit your quality systems, conduct clinical trials, prepare for inspections and file regulatory submissions in order to bring your products to market.
Clinical Trial Support
NSF provides efficient, effective clinical trial support and product development strategy. We help you optimize time and cost throughout the process while maintaining the highest levels of quality, integrity and scientific excellence.
Global Regulatory Strategy and Submissions
Receive your customized regulatory strategy from our team of former regulators and technical experts to efficiently bring innovative medical devices, in vitro diagnostics and combination products to market.
Schedule a mock audit or readiness inspection to prepare your team for the regulatory audit and inspection process. Our team of former FDA and MHRA regulatory inspectors provides detailed feedback, strategic advice and inspection support. If requested, we include “hats-on, hats-off” services.
NSF offers a variety of mock audits to help you ensure regulatory readiness. Assess a wide range of regulatory requirements to identify areas of risk and perform due diligence activities, or rely on NSF to support your internal and supplier audit programs.
Insights and Expertise
To ensure impartiality, use of NSF management systems consulting services or attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.