Pharma Resources
Check out the latest resources for Pharma.
Filter By Category
All Latest Resources
-
Overview of NSF’s Pharma Biotech Services
- 7 months ago
Get an overview of NSF's pharma biotech services, including consulting and regulatory affairs, auditing and education.
-
NSF Training Courses by Topic
- 7 months ago
This flyer includes some of our most popular training courses. For more information, or if you have a specific request, please get in touch with our team.
-
Webinar: A Structured Approach to Improving Investigation Report Writing
- 8 months ago
Did you know that inadequate investigations are the most often cited issue in FDA warning letters? This webinar from expert Andy Barnett addresses the most frequent investigation gaps cited by...
-
Regulatory Radar: FDA Regulatory Initiatives: What’s Ahead Based on the Spring 2018 Unified Agenda
- 8 months ago
The U.S. General Services Administration’s Spring Unified Agenda, released in May 2018, provides insight into upcoming FDA regulatory actions. Federal agencies including the FDA are required to publish an Agenda...
-
Webinar: IPSE’s Cultural Excellence Report and How It Changes Our Current Thinking
- 8 months ago
This webinar from expert Rachel Carmichael provides an introduction to ISPE's Cultural Excellence report. NSF views the culture of an organization as what your people will do when no one...
-
Webinar: Using Behavioral GMP to Create Perpetual GMP Inspection Readiness
- 9 months ago
How do the best companies remain inspection ready by design rather than good fortune? In this webinar, John Johnson covers what perpetual GMP compliance means and details how you and...
-
Webinar: Regulatory Perspectives on Data Integrity
- 9 months ago
This webinar from NSF expert George Toscano covers the trends and priorities when assuring data integrity from the perspectives of the U.S. FDA, MHRA and other regulatory bodies. George also...
-
Regulatory Radar: FDA Close to Approving First Marijuana-Derived Drug Product
- 9 months ago
An FDA expert panel was recently called upon to review a new drug application (NDA) by GW Pharmaceuticals for its product Epidiolex® containing the purified extract cannabidiol (CBD) from the...
-
Case Study: Preparing for a Regulatory Inspection
- 9 months ago
Learn how we helped a company prepare for a regulatory inspection. The key message that came from the project was that you need to approach inspection preparation in an open...
-
White Paper: Data Integrity - A Closer Look
- 9 months ago
NSF conducted extensive research into warning letters issued from 2005 to 2017 for data integrity deficiencies. In this white paper, George Toscano takes a deeper look into where companies were...
-
White Paper: Hierarchy for CAPA Effectiveness
- 9 months ago
Have you ever reviewed an investigation report and wondered whether the proposed corrective and preventive action (CAPA) would be effective? We propose our CAPA hierarchy to help investigators select an...
-
White Paper: Review of EU ATMP GMP Guidance
- 9 months ago
In this white paper, Robert Smith provides a deep review of the EU advanced therapy medicinal products GMP guidance that comes into force on May 22, 2018. Robert outlines what...
-
White Paper: The Future of the Pharmaceutical Industry
- 9 months ago
In this white paper, Martin Lush explains his view of the future of the pharmaceutical industry, and provides some key facts and essential back-to-basics advice on how you can prosper...
-
NSF Pharma Journal: Getting Back to Basics, Issue 41, 2018
- 9 months ago
This edition of the Journal includes insight from Martin Lush on the future of the pharmaceutical industry, an article on data integrity issues drawing on years of research and a...
-
Webinar: New Approaches to Validation; Trends and Best Practice
- 10 months ago
How do you design a risk-based and cost-effective validation program to meet cGMP expectations? This webinar provides an overview of the new science and risk-based approach to validation that is...
