Pharma Resources
Check out the latest resources for Pharma.
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Latest Webinars
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Webinar: Key Topics When Auditing a High-Speed Packaging Facility
- 3 weeks ago
Auditing a high-speed packaging line sounds easy and is something that many auditors can do, but how do you get to the heart of where the problems might be? In...
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Webinar: The UK Qualified Person – Best Practice for Gaining Eligibility
- 2 months ago
To gain Qualified Person (QP) status in the UK, candidates must apply to one of three professional bodies (the Royal Society of Biology, the Royal Society of Chemistry or the...
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Webinar: What Do Regulators Check for When Auditing Cleaning and Cleaning Validation?
- 3 months ago
In this webinar, David Waddington looks at the most common European and U.S. FDA regulatory findings related to basic cleaning issues including cross contamination and approaches to cleaning validation. He...
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Webinar: Introduction to the GMP Standard for OTC Drug Products
- 5 months ago
NSF/ANSI 455 defines the audit process and certification body requirements for OTC drugs’ GMP compliance. It was developed to establish a level playing field for certification bodies, reduce the audit...
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Webinar: Managing Contract Qualified Persons - What You Need From Them, What They Need From You
- 5 months ago
Becoming a contract QP can be daunting, especially if you are named on more than one licence. How do you maintain oversight of all the quality management systems and keep...
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Webinar: Hot Topics in the GMPs Used in Biotech and Biological Processing
- 5 months ago
Watch this webinar from NSF pharma expert John Johnson to learn what key subjects regulators focus on when auditing biotech facilities. Learn the top 10 concerns when interpreting, defining and...
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Webinar: How to Write a Contamination Control Strategy for Your Facility
- 8 months ago
How do I ensure my strategy for contamination control meets the new EU GMP Vol 4 Annex 1 requirements? How can I tell if it is well written, pragmatic and...
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Webinar: Implementing a Simplification Strategy
- 8 months ago
We all recognize the importance of simplifying pharmaceutical operations. This webinar reviews simplification strategies that site leadership and unit operations managers can pursue. You will learn: Standard operating procedure (SOP)...
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Webinar: Pharmaceutical Operations – What the Regulator Expects to See During a GMP Inspection
- 9 months ago
This webinar explores the key areas that regulators would expect to be under control at your pharmaceutical operations. These include cross-contamination control, facility layout, material/people flows, premises and equipment cleanliness,...
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Webinar: How to Install a Data Governance Process from Ground Zero
- 9 months ago
Since data integrity began to re-emerge as a serious issue around five years ago, companies have been asked to have a data governance system which MHRA has indicated should ensure...
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Webinar: Answers to Your Big Questions
- 10 months ago
What would you do if you knew you couldn't fail? This disruptive question shifts our thinking to a new way of working. This webinar from Martin Lush highlights the vital...
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Webinar: Managing a Pharmaceutical Quality Network, Real or Virtual
- 1 year ago
How do the best companies manage global pharmaceutical quality across a network or virtual supply chain? Lynne Byers explores different models for managing both internal company teams across a global...
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Webinar: Sharpening the Saw - How to Use Audits as a Way to Prevent Issues Becoming a Crisis
- 1 year ago
Watch this auditor training webinar from expert Mike Halliday. Learn how to use data from your auditing process to drive continuous improvement. You will also learn the key skills and...
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Webinar: How to Manage International Supply Chains Through Effective Outsourcing
- 1 year ago
More of us are turning to outsourcing, which is a major strategic decision that shouldn’t be taken lightly. There are many steps in establishing and nurturing a relationship with an...
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Webinar: Good Clinical Practice and Pharmacovigilance for QPs and QA
- 1 year ago
This webinar explores aspects of GCP and PV relevant to QPs and quality professionals. We cover what is different when releasing IMPs, what to be aware of beyond GMP, how...
