GMP Refresher Course 2023 On-Demand (Waiting List)
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As a pharmaceutical professional, it’s essential to stay up-to-date with the latest regulatory guidance and best practices to ensure the safety and quality of your products. It is also a requirement in all GMP regulations that all personnel working in such facilities are required to undertake continuing periodic training and assessment on the relevant duties assigned.
However, finding the time and resources to attend GMP refresher courses can be challenging. Our online on-demand GMP refresher course is the perfect solution for busy professionals who need to stay up-to-date with the latest regulatory guidance and best practices.
Our course covers all the essential topics, from basic concepts to the latest trends in regulatory guidance and hot topics like deviations and effective QMS. And best of all, our course is flexible and accessible on-demand, so you can fit training into your busy schedule without disrupting your work or personal life. Don’t let scheduling challenges hold you back from prioritizing your education and ensuring compliance and quality in the pharmaceutical industry.
Additionally, you will be eligible for our Q&A and bi-weekly discussion sessions with our Expert, Charley Maxwell.
Sign up for our comprehensive online on-demand GMP refresher course today and take control of your knowledge and skills in the field.
Who Should Attend:
- Everyone who is working in a GMP environment.
- Skill Level: Novice, Intermediate , Expert
- What is GMP?
- Recent Trends in Regulatory Guidance
- Basic Concepts of GMP
- Recent Regulatory Changes
- Regulatory hot topics
Special event information:
- Live Q&A with Charley Maxwell after Course Completion
Charley MaxwellManaging Director & Consultant QP / RP
Charley is the owner and Managing Director of Orion GXP Consulting. He has over 20 years of experience working in manufacturing QA, regulatory compliance, batch release, and distribution in the pharmaceutical and medical device industry. He has assisted multiple clients with designing, developing, and implementing phase-appropriate Quality Management Systems, vendor management, audit programs, quality risk management, and training. Charley has a Bachelor’s of Science In Biochemistry and a Master’s In Pharmaceutical Manufacturing Technology. He has acted as a QP in Ireland for sterile and non-sterile manufacture, clinical IMP release, and third-country Importation.
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If you attend the live session you will get a digital certificate of attendance emailed to you within 7-working days.
Yes, our event partners will email you the event recording within several weeks.