NSF Health Sciences Journal: Time to Rethink - Issue 47, 2020
We offer full contract research organization (CRO) services around the globe.
Our leadership team has significant expertise in biomedical research. We design and conduct clinical trial research projects in many therapeutic indications, including wound healing, oncology, CNS, diabetes, cardiovascular disease, infectious diseases and more.
We also support all stages of product development, including clinical development and manufacturing, addressing pharmacovigilance issues as they arise.
We'll take your product through the entire approval process, from creating the regulatory approval strategy to conducting trials and writing the marketing approval application.
We offer comprehensive services in project management (Phase I-IV, BE/BA and PK/PD), regulatory affairs (FDA applications and meetings, applications to international health authorities and GxP compliance audits), clinical operations, adaptive study designs, statistical analysis, data management, medical monitoring, safety and pharmacovigilance and general consulting.
Our team of regulatory experts guides you from strategy to approvals. NSF works with regulatory authorities around the world, and we consider regulatory strategies at every step of the way to minimize timelines and improve the chances of success for your product registration. During your company's interactions with global regulatory agencies, our team of former FDA regulators provides superior representation, strategy and support.
Our submission strategies support early clinical development, product registration and late-phase trials in a global setting.
Backed by more than 20 years of industry experience, our team develops customized submission strategies designed to save you time and money. Receive expert guidance throughout your entire project lifecycle in order to meet regulatory standards for electronic submissions and prepare and deliver your application with confidence.
Our services also include:
We have helped obtain the following market approvals:
Contact us with questions or to receive a quote.
NSF Now Offering Live Instructor-Led Virtual Pharmaceutical and Medical Devices Training
May 19, 2020
To complement its face-to-face offering, NSF now offers traditional classroom courses as virtual instructor-led training to support your professional development. Courses are delivered via a combination of live instructor-led virtual classrooms and self-paced online learning. NSF’s coaches are on hand to guide participants through the interactive sessions which also include pre- and post-course activities.
NSF International’s Health Sciences Team Joins Fight to Save Lives With More Ventilators
April 23, 2020
NSF International’s health sciences team is hands-on in the rapid ventilator manufacturing specification issued by the United Kingdom (UK) government. The UK National Health Service needs thousands more ventilators to help save lives as the country’s COVID-19 pandemic approaches its expected peak and ventilator capacity becomes a challenge.
The Spectrum of Food Safety Audits: Remote Audits, On-Site Audits and the Future of Real-Time Monitoring
October 21, 2020
NSF International Honors Food Safety Pioneer Dr. Jennifer McEntire at 2020 Food Safety Summit
October 20, 2020