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

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.

9 July 2024 »

Need help?  Enrol or reserve

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. For more information on the latest EU GMP regulations, see our GMP training course covering the Annex 1.

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)

Enrol or reserve

The The Latest Updates in Global GMP course will cover:

  • Brief History of GMP
  • APIC, USP, ICH Updates
  • PIC/S, FDA, EMA, MHRA, WHO and Other Health Authority Updates
  • Q&A Session

Enrol or reserve

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

NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:

  • 30% off the 2nd delegate*
  • 40% off the 3rd delegate*
  • 50% off the 4th delegate*

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

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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.

Egypt

  • Mash premiere
  • Otsuka
  • Otsuka for pharmaceutical industry
  • Sedico

Portugal

  • Owlpharma
  • Próprio
  • ValGenesis

Turkey

  • Accenture
  • Atabay
  • Cinnagen İlaç

India

  • Dr.D.Y.Patil Institute Of Pharmaceutical Sciences And Research, Pimpri, Pune

Iraq

  • Kmca

Tunisia

  • VITAL

United Kingdom

  • Student

United States of America

  • Cardinal Health

Enrol or reserve

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:

Run this course conveniently and cost-effectively in-house for your staff and colleagues

Aleksandra Beer

Aleksandra BEER
Training expert

Yesim Nurko

Yesim NURKO
Training expert

+44 (0)20 7749 4749

inhouse@ipi.academy