|26 - 28 Sep 2016||Barcelona||Spain||
Mr. Nigel D. Lenegan|
|7 - 9 Nov 2016||Tampa, FL||USA||
Mr. Norman A. Goldschmidt
The course focuses on common issues and problems in the operation of a facility and maintaining readiness for cGMP inspection. Topics include control system alarm management, common system construction deficiencies, cGMP documentation, maintaining an "inspection ready" state, frequency of testing and balancing, airflow visualization, air change rate reduction and more.
Participants will review global cGMP regulations, as well as common interpretations of those regulations and how they may apply to their facilities. The class will explore critical issues at each stage of the product lifecycle, from R&D to Manufacturing, such as: controlling cross-contamination between products, determining the correct classification of spaces, proper control of storage temperature and humidity, setting acceptance criteria for HVAC systems and using risk assessment to set environmental criteria. Workshops that include templates will be provided to help participants immediately apply what they have learned.
The course also examines the challenges and some accepted HVAC solutions for a variety of facility types, including: Laboratories, Bulk Pharmaceutical Chemicals (BPC), Bulk Biologics, Vaccines, Oral Dosage Forms (solid and liquid), Sterile fill/finish, Medical Devices and Combination Devices.
Since HVAC systems can account for as much as two thirds of the energy usage in pharmaceutical facilities, system design and critical parameter selection for efficiency will be explored for all facility types. Workshops are provided on the sustainability impact of choices made during design to provide participants with ready examples of efficiency evaluation to use in their own facilities. On completion of facility-specific systems, the requirements for verification or commissioning and qualification are explored with emphasis on distinguishing between critical and noncritical equipment and parameters.
Note: The course focuses on leveraging a solid understanding of the properties of air, HVAC and contamination control principles to assure control of critical environments.
Immediately apply the course learning objectives with the complimentary copy of the ISPE Good Practice Guide: Heating, Ventilation, and Air Conditioning.
This training course is of particular interest to existing and future members of the ISPE HVAC Community of Practice (COP).
ISPE will provide continuing education units (ISPE CEUs) for all North American and European courses. CEUs are nationally recognized units of achievement designed for those individuals continuing their education in their chosen field or profession. Verification of CEUs is based on attendance as well as satisfactory completion of all evaluation materials. Statements of credit will be available for download in your ISPE account within four weeks of the completion of training. Instruction for download will be sent when the CEUs are available. One hour of education programming equals 0.1 ISPE CEU credits.
Implementation of the Lifecycle Approach to Process Validation Statistics
Monday, 29 Aug 2016 17.08
Meet 2016 – 2017 ISPE International Board of Directors
Wednesday, 24 Aug 2016 19.08
Biotechnology Manufacturing – Transforming Healthcare for Millions
Tuesday, 23 Aug 2016 13.08