Presented by
Management Forum
In this free 90-minute webinar, you will gain an insight into the latest updates in GMP, as well as consolidating your existing knowledge on the subject.
With this distinguished GMP Update training, EMA, PIC/S, FDA, WHO, ANVISA, MHRA, etc. all sections that will be updated in the GMP Guide, all the innovations in the concept papers, draft articles, and the latest developments in the International GMP Guides will also be processed.
Many pharmaceutical manufacturers tend to describe GMP practices as the rules that personnel must comply with throughout production and the recording of production steps. However, GMP is a comprehensive set of rules in which the steps to be followed in all processes, including the production of pharmaceutical products and R&D activities throughout the product life cycle, are validated and recorded. GMP disasters throughout history have caused indelible tragedies in many companies. Every country that considers patient health and safety as the priority allows the production, import, and sale of pharmaceutical products per the internationally recognised current GMP rules. GMP (Good Manufacturing Practices), a concept established in the terminology of Good Manufacturing Practices, generally appears as cGMP (current Good Manufacturing Practices) supported by the FDA. The letter c added to the beginning of GMP means "up-to-date" and refers to constantly updated and living rules, apart from the "apply and produce what is available" logic of GMP, and even the health authority reminds the manufacturer that they must constantly stay up-to-date.
This course is part of our GxP training (Good x Practice) course collection, which features a variety of topic areas to ensure you comply with the most recent quality guidelines. For more information on the latest EU GMP regulations, see our GMP training course covering the Annex 1.
Mustafa Edik is an Independent GMP Consultant and Auditor.
After graduating as a Chemist from university, Mustafa began his 25 year plus career as a Laboratory Supervisor at Bayer, a German Pharmaceutical Company. After 15 years of working as a Quality Assurance Assistant Manager, Laboratory Supervisor, Pharmaceutical Quality Management Systems, and GMP Lead Auditor, he decided to continue his career as a Consultant. He has served the Turkish Atomic Energy Authority (TAEA) as Principal GMP Auditor and Consultant for 6 years. TAEA was audited by the Republic of Turkey Ministry of Health and granted GMP Certificate for 5 Radiopharmaceuticals. This success has won great acclaim from all health authorities and industry.
He has prepared and presented various training courses and workshops to more than 8000 individuals from 150 International and local Pharmaceutical, Medical Device, and Cosmetics companies on GMP, GDP and Pharmaceutical Quality Management Systems. He has taken part in several International Pharmaceutical Facility Establishment projects as GMP Consultant and has also set up various Quality Management Systems for Local Pharmaceutical and Medical Device Companies.
While he was the Vice President of Quality and Technical Operations at a Quality Academia Training and Consultancy firm, he acquired and converted it into a 100 % Turkish Company. As the only IRCA Certificated Pharmaceutical Quality Management Systems and GMP Lead Auditor in Turkey, he currently conducts API, Excipient, Packaging Materials Suppliers and Manufacturers, Third Party Logistics Service Providers, Sterile and Non-Sterile Manufacturing Facilities Audits according to FDA, EMA, PIC /S, TMMDA, MHRA, TGA Health Canada, and WHO regulations and guidelines.
He finished his second university degree in Biopharmaceutical Sciences BSc (Hons) at Atlantic Technological University - Ireland. He is the author of chapter 6 of the book published by PDA named “Good Distribution Practices” and his new book on ‘GMP Audits in Pharmaceutical and Biotechnology Industires’ will be published by Taylor & Francis in June 28, 2024.
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
Please contact us for pricing if you are interested in booking 5 or more delegates
9 July 2024
Free + recorded
Live online
14:00-15:30 UK (London) (UTC+01)
15:00-16:30 Paris (UTC+02)
09:00-10:30 New York (UTC-04)
Course code 15192
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
Turkey
India
United Kingdom
United States of America
Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to: