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The Latest Updates in Global GMP (Good Manufacturing Practice) Training Course

Free

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.

★★★★★ "Thank you"

Recorded on 9 July 2024 »

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Course overview

This webinar will provide the latest GMP updates which are supported by the following health regulatory authorities: EMA, PIC/S, FDA, WHO, ANVISA, MHRA, etc. and will address all sections that will be revised in the GMP Guide. Concept papers, draft articles, and the latest developments in the International GMP Guidelines will also be discussed.

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, regularly appears as cGMP (current Good Manufacturing Practices) and is encouraged and supported by the regulatory authorities who often remind the manufacturer that they must constantly stay up-to-date.

This webinar will provide an essential update on the latest changes and ensure you are cGMP ready.

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.

Benefits of attending

Refresh your existing knowledge surrounding GMP practices
Learn the latest updates in cGMP, including guidance from the EMA, PIC/S, FDA, WHO, ANVISA and MHRA
Explore the latest innovations in the concept papers, draft articles and the latest developments in the International GMP Guides

Who should attend

Quality assurance personnel
Quality control personnel
GMP compliance personnel
Manufacturing personnel
Supply chain/logistics personnel
Regulatory affairs personnel
Engineering personnel
IT personnel
Regulatory authority inspectors/auditors (human and veterinary medicinal products)

Mustafa Edik

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.

More details

Recorded on 9 July 2024

Free

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

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Reviews of IPI's The Latest Updates in Global GMP training course

Thank you

Jul 9 2024

Pranav Jogani India
Freelancer, Pranavjogani& Associates

Jul 9 2024

5*. Good.

Roshan Umale India

Jul 9 2024

Very good content.

Markus Wollenweber Switzerland
Owner, Wollenweber GMP/GDP-Services

Jul 9 2024

I [particularly] liked the historical data presented. Thank you!

Nieza Jane Patna Philippines
Research and Development Officer, Xylem Bio-Solutions Inc.

Jul 9 2024

He was very clear, precise and I understood everything. He is good speaker

Tasmiya Banu India
Student, Mount carmel college

Jul 9 2024

The entire presentation was upto the mark, the presenter, presentation and support team have been very generous and helpful. Special thanks to entire team for efforts. I look forward to more such insightful webinars with IPI academy

Devyani Shinde India
Quality control officer , -

Jul 9 2024

The content was very good as it requires for a webinar. The presentation was neat and clear. Dr. Mustafa Edik speech is good enough.

Maria Livin Arul Oli A India
Student, KIT-Kalaignarkarunanidhi Institute of Technology

Jul 9 2024

Professional Excellent Knowledgeable

Iqra Rukhsar United Arab Emirates
Pharmacist , Pharmacy

Jul 9 2024

It was excellent

Sara Sangam India

Jul 9 2024

I was indulged throughout the webinar. Loved everything.

Gunjan Jain India

Jul 9 2024

I think the webinar is perfect as it is and I will definitely look to book onto future ones with IPI Academy.

Joanna Fox United Kingdom
Regulatory Compliance Trainer, ITS Ltd (Industrial Technology Systems Ltd)

Jul 9 2024

Overall the webinar was very knowledgeable and the content was well explained and speaker has gives good motive to need to learn more about GMP updates .

Mamta Saganali India

Jul 9 2024

In one word I would say I got too much new information so it was excellent

Rutvik Parikh India
Student , Parul university

Jul 9 2024

It was a Wonderful and Informative Session

Sagunthala KT India
Student, Cauvery College for Women (Autonomous)

Jul 9 2024

It was extraordinary

Sruthi M India
Polymer engineer, Ion exchange

Jul 9 2024

Incredible

Enayah Alshanawani Saudi Arabia
Fresh Graduate, N/A

Jul 9 2024

Overall the presentation was amazing.

Boopal Raj India
Sas programmer, Clri

Jul 9 2024

Very good

VISHWAJIT LEWADE India
Pharmacist , SPPU, Pune

Jul 9 2024

Well organized.

Teoh Meng Hong Malaysia
QA Manager , Goh Siong Tee Marine Product Sdn Bhd

Jul 9 2024

Understanding Regulatory Updates: I aimed to gain insights into the latest regulatory changes and guidelines in our industry. The webinar provided detailed updates on recent regulations, which were extremely informative. I now have a clearer understanding of the new requirements and how they impact our compliance processes. Overall, I believe I accomplished my goals. The webinar was well-organized and delivered on its promises

Joana Costa Portugal
Regulatory Affairs Trainee, --