GMP for Clinical Trials Manufacture and Supply Training
About This Course
Keeping up with the changing legislation for clinical trials provides challenges for all those working with investigational medicinal products. This highly interactive training course teaches you all you need to know about international GMP regulations and requirements for the manufacture, control, storage and distribution of medicines to be used in clinical trials manufacture.
Using practical exercises, our clinical trial GMP training tutors help you to gain a better understanding of the ever-changing world of clinical supply and its legislation. Our tutors are a combination of ex MHRA inspectors and current IMP QPs, and teach you simple and pragmatic ways of working designed to help you better meet the needs of the regulators.
This training will be delivered as a combination of an instructor-led virtual classroom and self-paced learning online. Full details will be sent to you following registration.
This course is approved by the Royal Society of Chemistry and is suitable for its members’ continuing professional development.
Key Learning Objectives
On completion of this course, delegates will know and understand:
- The legislation and guidance around clinical trials and what is changing
- The interpretation of GMPs suitable for clinical trials
- The phases in clinical trials and how requirements change
- Auditing and control of clinical trial operations
- The areas of interface between GMP and GCP requirements and how these should be managed
- Clinical batch releases
Course Outline
Clinical Trials
- What are they?
- Phases of clinical development
EU Legislation Impacting Clinical Supplies
- Annex 13 and Clinical Trial Regulation 536/2014
- GMP Regulation 2017/1569 for IMPs
EU and FDA expectations compared Good Manufacturing Practice for Clinical Manufacture
- Risk management
- Sourcing of materials, including comparators and supply chain management
- Production and quality control of IMPs
- Documentation
- Packaging issues (labelling, blinding and product security)
- Validation (how much, how soon?)
- Assigning and extending shelf life
- Retains and returns
- Assessing “equivalence” of GMP standards
- Quality/technical agreements
Good Clinical Practice
- What is GCP?
- The GMP/GCP interface
Release Procedures and the Role of the QP
- QP responsibilities
- Two-stage release process
- Key challenges
The GMP/GCP Interface
- Issues that fall in the interface
- Audit findings in this area
Shipment to Clinical Sites
- Cold chain supplies
- Transportation
Typical Regulatory Inspection Findings
Discussion and Working Groups
A significant portion of course time is devoted to group work. Using case studies, delegates have the opportunity to put theory into practice. In addition, discussion periods (which include a course tutor panel session) provide delegates with an opportunity to obtain answers to their specific question and concerns.
Who Should Attend
The Aspiring Qualified Person
- Our training is generally considered the best available and our QPs are held in high regard in the industry
- As well as being accepted in the UK, our training courses are well known and accepted by several other EU countries including Ireland, the Netherlands, Austria, Hungary and Malta
- You are more likely to become a QP with us than with any other training provider
The Pharmaceutical Technical Professional
- Not all the people attending these courses intend to become QPs. Many use the training to develop as technical managers in other areas of pharmaceutical manufacture and control
- Many industry professionals from a range of disciplines attend the courses as part of their continuing professional development. Taken with some of our other QP modules, this course is designed to lead to postgraduate certificate, diploma and MSc qualifications
Course Tutors
Darren Jones – Darren is an ex-MHRA GMP Inspector and has audited dosage forms for both commercial and clinical trial applications. Darren also has a wealth of practical knowledge and experience applying GMP in the clinical development world gained during his 18 years with AstraZeneca, prior to joining the MHRA. He was a Qualified Person for IMPs and knows the real challenges and how to overcome them.
Richard Funnell – Richard spent 11 years with the MHRA, including seven as a Senior GMP Inspector with the lead for IMPs. Richard has current knowledge and understanding of what inspectors are looking for in the lead up to the new clinical trial regulations.
Kate Krachai – Kate has over 20 years’ experience in the pharmaceutical industry as a proactive quality manager and pharmaceutical lead auditor, working to enrich quality systems and compliance with companies of varying sizes globally.
Discounts
Multi-delegate discounts available. Discounts also offered to NHS staff and charities.
Pharmaceutical Quality Systems
Pharmaceutical Law and Administration
The Role and Professional Duties of the Qualified Person
Additional Recommended Courses
Mathematics and Statistics
There are many training courses on statistics and statistical analysis, but very few which focus specifically on the application of these techniques to pharmaceutical manufacture and control. This is one such course! Designed to meet the needs of the aspiring Qualified Person and other pharmaceutical professionals and taught by a combination of statisticians and pharmaceutical industry professionals, this highly participative four-day mathematics and statistics pharmaceutical training course will teach you how to use statistical techniques to assess and monitor the reliability and accuracy of data you generate and the capability and reliability of the processes you work with. A pharmaceutical statistics course like no other! 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: To be confirmed
Price: £3160 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).
Pharmaceutical Microbiology
A highly interactive pharmaceutical microbiology training course, designed to provide you as an aspiring Qualified Person and pharmaceutical quality professional with the knowledge and understanding you need to: assess microbiological risks in the pharmaceutical manufacturing environment, assist in the design and implementation of comprehensive microbiological control strategies, and also so take informed decisions when microbiological problems occur.
Tutors: To be confirmed
Price: £3160 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 and NHS staff are entitled to a 50% discount. (Proof will be required).
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).