Pharmaceutical Training
Known globally for their high-quality content, our pharmaceutical courses have the depth, range and flexibility to meet all your needs.
Download our PDF guide to view all our training courses in one place.
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Certificate in Pharmaceutical Quality
Certificate in Pharmaceutical Manufacturing
Auditor Training
GxP Training
Qualified Person Training
Quality Systems Training
Regulatory Training
Sterile and Biotech Training
Qualification and Validation Training
Other Technical Training
Pharmaceutical Legislation Update
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Featured Courses
Pharmaceutical GMP
This highly interactive virtual pharmaceutical GMP training course will teach you how to apply pharmaceutical GMP in your workplace and keep you up to date with industry requirements. The course provides an excellent opportunity to share your GMP questions with experienced industry experts and hear their solutions first-hand.
This virtual instructor-led training course is delivered over two consecutive days and will be managed through our online Learning Management System. Full details will be emailed following registration.
Tutor: To be confirmed
Price: £780 excluding VAT (where applicable)
Please note: payment by credit/debit card will be required at time of booking.
You can view our booking terms and conditions from here.
Compliance to Performance
NSF will host its second Pharma Biotech conference on 14 November at The Royal Society of Chemistry in London.
We will be welcoming a range of speakers from industry, regulatory bodies, and industry associations. Speakers include:
Christopher Davenport – AstraZeneca
Lynne Ensor – NSF
Paul Fleming – British Generic Manufacturers Association/British Biosimilars Association
Dr Peter Gough – NSF
Dr Richard Greville – Association of the British Pharmaceutical Industry
Emilija Matelyté - The European Medicines Agency
Liam Rogers – NSF
Bruce Warner - RPS and Former Deputy Chief Pharmaceutical Officer for England
The two themes for the one-day event are artificial intelligence (AI) and the technological advancements in manufacturing and supply chain shortages and resilience.
09.00-10.00 Registration, Coffee, and Networking
Morning Session 1
In this initial session Pete Gough will provide a comprehensive regulatory update, with a focus on our two conference themes. Following this we will hear from industry experts about their experiences of AI and technology advancements, with real life examples and thought-provoking initiatives that will keep the discussions flowing throughout the networking break.
Networking Break
Morning Session 2
The second morning session will focus on the impact of artificial intelligence and how it, and other technologies, are shaping regulation and activities across the pharma biotech sector.
Christopher Davenport from AstraZeneca will look at how the industry has responded to the breakneck speed of developments in recent years. Liam Rogers from NSF will look at the issue from his perspective of working with our clients across clinical, medical device, and pharma biotech, and consider how the technology is being adopted.
Networking Lunch for delegates and speakers
Afternoon Session 1
The afternoon session focuses on the issue of supply chain. The past 5 years have brought this topic onto the front page of newspapers and TV news bulletins. The issue of supply chain resilience is of critical importance to the pharma biotech sector.
Emilija Matelyté from The European Medicines Agency will be joined by Bruce Warner to look at issues around supply and availability from a European perspective.
The afternoon session will also hear from two of the most respected names in pharma biotech industry associations. Both Paul Fleming and Dr Richard Greville will discuss how companies are dealing with disruption and building resilience into their supply chains.
The day will end with a questions and answers session between guests and speakers. Last year’s event had a vibrant questions and answers session and the 2024 event is sure to spark several topics for delegates and speakers to consider.
16.30 Closing Remarks from Lynne Ensor.
You can purchase a ticket to attend by clicking the register button below or at the top of this page.
Analysis and Testing
This highly focused, intensive four-and-a-half-day course, taught by leading scientists and former Quality Control Managers, is designed to provide the aspiring Qualified Person or pharmaceutical quality professional with the knowledge and understanding they need to be able to perform their duties with skill and competence when interacting with the Quality Control laboratories.
We will explain to you the strengths and limitations of analysis and specific analytical methods, we will advise you on how to apply the principles of quality management and GMP to the testing environment in a pragmatic, effective way, and we will advise you of the very latest “hot topics” with the regulators and how to ensure that your laboratories are in compliance.
This virtual blended training course will be delivered via a combination of an instructor-led virtual classroom and self-paced learning online. This will require an element of learning to be completed prior to the virtual classroom, as well as afterwards and this will be managed through our online Learning Management System. Full details, including timings for the instructor-led virtual classrooms, will be emailed following registration.
Tutors: Dave Waddington, Oona McPolin
Price: £3555 excluding VAT (where applicable)
Course registrations will close 5 working days before the start of the course.
You can view our booking terms and conditions from here.
Multiple Delegate Discounts are available for delegates from the same company attending the same course.
The first delegate must pay full price. The second delegate will receive a 20% discount. The third and any subsequent delegates will receive a 50% discount. Charities, NHS staff are entitled to a 50% discount. (Proof will be required).