Approved training courses
You can register for this service all year round. Pharmaceutical legislation and regulatory authority guidance are continually changing. These changes, and their interpretation, can have significant implications for companies. Many changes require detailed planning to implement and failure to do so can result in serious compliance problems.
This pharmaceutical regulatory training provides you with 12 months of updates of changes to legislation and guidance that have the potential to impact the manufacture and distribution of medicinal/drug products. A full update for the past year and a summary of what is new each quarter will be provided in in February, May, September and late November. Your subscription will start with the next available update. The updates will be provided as recordings through NSF’s online LMS portal and can be viewed at a time convenient to you. To access the recorded updates, we will create an account for you on our LMS and, as each update is made available, you will receive an enrolment email giving you a link to access the material. There will also be an opportunity for Q&A through a live two-hour virtual meeting each quarter.
This training provides essential information for Qualified Persons and other quality professionals employed by organizations that manufacture or distribute medicinal/drug products.
Key Learning Objectives
To understand and discuss the current interpretation of recently implemented and proposed changes to legislation and guidance which has the potential to impact the manufacture and distribution of medicinal products. This includes changes from:
• EU medicines legislation: Directives and regulations
• EU GMP guidance
• The impacts of Brexit on biopharmaceutical processes and supply chains across the EU and the UK
• ICH guidance
• US drug legislation and FDA guidance
• UK medicines legislation and MHRA requirements and processes
Who Should Attend
• Quality assurance personnel, Qualified Persons
• Other technical/managerial personnel responsible for the manufacture and testing of APIs and medicinal products
For any queries regarding entry requirements for both QP training and/or postgraduate qualifications please contact QPpharma@nsf.org
Additional infoNSF delivers instructor-led QP courses with blended training methods, in a mix of virtual and in-person courses. Please visit www.nsf.org/training for current dates. If you cannot see your delivery method of choice, please contact QPpharma@nsf.org
Blended Learning
On request from training provider
£595.00 GBP (plus VAT)
Find an approved training course
Use the options below to search through the growing list of chemical sciences training courses that have been approved by the Royal Society of Chemistry.
Courses are approved for CPD purposes only; approval does not imply they will fulfill any regulatory requirements.
