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1st International Validation Week-Istanbul

1st International Validation Week-Istanbul

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Who should attend?

You will benefit from attending this event if you are working in the Pharmaceutical, Biotechnology, Medical Device industry with responsibilities in the following areas Senior VPs, VPs, Chief Scientific Officers, Directors, Managers, Professors, and Principal Investigators in: Validation & Qualification Analytical & Microbiology Laboratory Contract Laboratory R&D IT Quality Assurance & Quality Control Manufacturing & Operation Supply Chain Warehouses & Distribution Centers Engineering GMP Compliance Audit Regulatory Affairs Project Management Technical Operations Product Submission Formulation Tehnical Writing Metrology LIMS ERP Method Development Stability Training Process Development Regulatory Affairs

Details

1st International Validation Week organized by Quality Academia Training & Consultancy is the most extensive International Validation Event to be held in Istanbul on September 26-27-28-29, 2017 We are so proud to announce that this event is the most comprehensive one dedicated to validation in the pharmaceutical and biotechnology industries.

We aim to be the the forefront of delivering the best validation practice. New business models, new regulations, new technologies have helped pharmaceutical and biotechnology companies develop, implement, sustain validation procedures company-wide. This event will cover Process, Facility, Computer, Software, Equipment, Analytical Method, Cleaning, Microbiological Method, Risk Management, VMP, Change Control, Supplier Qualication Applications, and much more...

DO NOT MISS THIS OPPORTUNITY TO DISCUSS NUMEROUS TOPICS WITH YOUR VALIDATION, QUALITY, ENGINEERING, IT, AND MANUFACTURING COLLEAGUES ALL AROUND THE WORLD.

Best Regards

On Behalf of Event Producer

Mustafa EDIK / QA Vice President

 

WHY YOU SHOULD ATTEND THIS EVENT?

  • Understand strategies to design and implement a compliant validation program
  • Hear the latest regulations guidelines, including FDA, EMA, PIC/S and ICH requirements
  • Debate the best approaches for data management of validation & qualification data
  • Understand the importance of risk assessment Review current methods used to reduce costs
  • Explore the benefits of supplier qualification
  • Discuss challenges associated with data integrity
  • Use this opportunity as a platform for future collaborations

View the event e-brochure here

View the event webpage here

View the Quality Acidemia website here

Prices

FOR FURTHER INFORMATION PLEASE FELL FREE TO GET IN TOUCH WITH ; cenke@qualityacademia.com

Contact

CENK EROGLU
cenke@qualityacademia.com

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