Preparing for Market
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?
Audits and inspections assess the capability of an organisation to follow the relevant regulations, requirements and guidances.
Clinical Trial Support
NSF provides efficient, effective clinical trial support and product development strategy. We help you optimise time and cost throughout the process while maintaining the highest levels of quality, integrity and scientific excellence.
Preparing for GxP Inspections
Identify key risks and follow expert mitigation strategies prior to your GMP inspection. We'll help you prioritise and address concerns, creating perpetual inspection readiness.
Regulatory Strategy and Submissions
Receive customised regulatory pathways to bring innovative pharmaceuticals, biologics, gene and cell therapies and combination products to market efficiently.
Streamlining Pharma Operations in the Wake of COVID-19
NSF Health Sciences Journal: Time to Rethink - Issue 47, 2020