Pharma and Biotech Support

We support you throughout the product lifecycle with the development, manufacture and delivery of safe and effective products. NSF helps you bring your products to market cost-effectively and time efficiently.

Our global consulting experts, including former regulators and industry experts, help pharmaceutical and biotech companies establish or remediate quality systems, mitigate risks and achieve sustainable compliance.

• Developing and Improving Quality Management Systems

  Create robust quality systems and ensure international GMP compliance with the support of NSF's former regulators and industry experts.

• Getting Results

  Respond to adverse regulatory inspection findings, build a compliant quality system and avoid future problems with a custom remediation plan.

• Preparing for Pharma and Biotech Market

  Prepare for market launch by conducting clinical trials, developing regulatory filing strategies and ensuring inspection readiness.

• Training and Education

  Bring about change that drives improvements.

We Offer Custom Training

The Right Training for Your Team

Our interactive training courses are based on real-world scenarios and designed to help you meet international requirements, no matter where you are located.

Learn more about our training

News and Events

May 2023 Pharma News Update

May 8, 2023

This month we have a bumper news update with developments from the FDA, EU, MHRA, and the ICH.

March 2023 Pharma News Update

March 1, 2023

The U.S. NIST has developed a framework to better manage risks to individuals, organizations and society associated with artificial intelligence (AI).

Meet NSF Pharma Experts in 2023

February 9, 2023

Our pharma experts are attending and speaking at some of the top pharma conferences in 2023. Book a meeting.

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.

See More News