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Preparing for Pharma and Biotech Market

Get ready for market launch by conducting clinical trials, developing regulatory filing strategies and ensuring inspection readiness through training and auditing.

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 to bring your products to market.

How Can We Help?

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.

Pharma and Biotech Industry Audit Services

Audits and inspections assess the capability of an organization to follow the relevant regulations, requirements and guidances.

Preparing for GxP Inspections

Identify key risks and follow expert mitigation strategies prior to your GMP inspection. We'll help you prioritize and address concerns, creating perpetual inspection readiness.

Regulatory Strategy and Submissions

Receive customized regulatory pathways to bring innovative pharmaceuticals, biologics, gene and cell therapies and combination products to market efficiently.

Resources

Streamlining Pharma Operations in the Wake of COVID-19

COVID-19 is shedding further light on pharmaceutical sourcing strategies and their inherent complexity. Jim Morris highlights vital areas that will warrant leadership attention to streamline pharma operations in a COVID-19 environment, including supplier oversight, inspection readiness and the impact on personnel.

NSF Health Sciences Journal: Time to Rethink - Issue 47, 2020

This edition of the health sciences Journal is about hope and optimism, and how we must rethink our ways of working.

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News and Events

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.

Brexit Implications for the UK Pharmaceutical Industry

January 3, 2018

The only thing that is certain following the UK’s momentous decision to leave the European Union (EU), so called Brexit, is that the pharmaceutical industry, as all others, is facing at least two, and probably many more, years of unprecedented uncertainty.

February 2023 Pharma News Update

February 1, 2023

The U.S. fiscal year 2023 appropriations bill has introduced new measures for the FDA. Find out what they are in the February 2023 update.

NSF Launches 229 China GMP for Nutritional Supplements

January 9, 2023

New Certification Standard Combines China GMP and National Product Safety Standards with U.S. FDA GMP Requirements to Meet Demands of Supplement Manufacturing in China.

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