|7-8 October 2013||New Brunswick, New Jersey||USA||Jeffery Odum|
This course provides an overview of the concepts utilized in the development of sound designs for facilities that manufacture pharmaceutical products in today's regulatory environment. The course will include a review of facility design and regulatory issues in the U.S. and Europe that involve industry trends and changing regulatory policy.
The course will include current case studies on a wide array of facility topics as well as a class exercise in developing a facility scope of work and deliverables.
This course includes a pre-recorded Webinar that provides a review of the basics prior to the classroom course. You will receive information via email on how to access the Webinar one week prior to the start of the training event.
This course contains knowledge related to the CPIP™ technical knowledge competency element Facilities and Equipment: Design and Construction / Installation. For complete information concerning the knowledge elements or the CPIP Credential, please visit www.ISPE-PCC.org.
ISPE will provide continuing education units (ISPE CEUs) for all North American seminars and courses, including educational programming at the ISPE Annual Meeting. CEUs are nationally recognized units of achievement designed for those individuals continuing their education in their chosen field or profession.
Delegates attending European seminars and courses will receive a Certificate of Attendance, as ISPE CEUs are currently not offered at European events. Verification of CEUs is based on attendance as well as satisfactory completion of all evaluation materials. Statements of credit will be sent via email within four weeks of evaluation materials. One hour of education programming equals 0.1 ISPE CEU credits.