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EVENT DATES
Dec 2016
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Venue

Venue TBD Washington , District of Columbia
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Effective Design, Validation and Routine Maintenance of Pharmaceutical Gases

30 0

Overview

Pharmaceutical gases such as Compressed, Nitrogen Argon gas systems used for the production of finished pharmaceutical or other types of products may either have direct or indirect impact to the finished products. These gases are also used for other medical and non-routine processes hence understanding the design, validation, routine monitoring, data management, failure investigations, regulations and applicability of each type of gas system ensures compliance to the required regulations. A detailed technical understanding of how to perform these critical steps during the initial evaluation or re-evaluation of a new, modified or existing gas system will eliminate expensive failure or remediation issues, inability to perform validation as well as routine testing and maintenance issues which ultimately impact or delay the release of the affected product.

This 2 days seminar will provide the attendee an extensive technical and practical knowledge that includes the step by step process of evaluating a new gas system through the design, installation, validation, routine monitoring/testing, data management, performing a gas failure investigation, excursion or out of specification results and trending so as to avoid the high cost associated with a poorly designed system. This seminar contains a lot of technical content, case studies, practical discussions and an exciting learning environment.

Why you should attend:

This seminar will provide an enormous amount of technical information and will be beneficial to those involved in the establishment, design, installation, validating, testing, review and approval of a new and modified or existing pharmaceutical gas programs so as to meet the requirements of ISO 8573, USP or FDA requirements. It will also benefit the vendors and suppliers of pharmaceutical gases to ensure compliance to the different regulatory bodies’ requirements.

Who will Benefit:

This seminar will benefit those involved in manufacturing, using, testing and Validating pharmaceutical gas systems in various industries such as the Pharmaceutical, Biotechnology, Drug, Biologics, Medical Device and In-vitro Diagnostics Product Manufacturing Industries, especially:

  • Quality Assurance Personnel and Management
  • Quality Control Personnel and Management
  • Laboratory Managers
  • Testing Analysts and Technicians
  • Manufacturing Personnel and Management
  • Suppliers and Vendors of Pharmaceutical Gas Systems
  • Validation Personnel and Management
  • Supplier Quality Assurance Personnel and Management
  • Regulatory Affairs Personnel and Management
  • Shipping and Receiving Personnel and Management
  • Facility and Maintenance Personnel and Management
  • Microbiologist Personnel and Management
  • Engineering Personnel and Management
  • Materials Management Personnel and Management

Note:
Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

http://www.complianceonline.com/pharma-gas-programs-iso-8573-usp-fda-requirements-seminar-training-80432SEM-prdsm?channel=eventsinamerica

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