Event Schedule

Sunday
20 February
15.00 - 1730 Registration Desk Open
Monday
21 February
07.00 – 18.30 Registration Desk Open
07.30 – 08.45 New Member/First Time Attendee Orientation
07.30 – 09.00 Continental Breakfast
08.00 – 09.00 CPIP™ Introduction Workshop
09.00 – 17.00 Aseptic Processing of Sterile Products: Innovations, Regulatory Guidance and Compliance in a Practical World (E01)
Quality Risk Management: Focused, Practical Application (E02)
Data Integrity: How to Verify, Validate and Maintain (E03)
Inspection Readiness Workshop: From Site Preparation to Successful Execution (E04) (Cancelled)
Cleaning Validation Principles (T17)
Containment Fundamentals (T16) (Cancelled)
17.00 – 18.30 Exhibits Open
Opening Reception in Exhibit Hall
Tuesday
22 February
07.00 – 17.30 Registration Desk Open
07.30 – 09.00 Continental Breakfast in the Exhibit Hall
07.30 – 16.00 Exhibits Open
08.00 – 09.00 CPIP™ How-to Workshop
09.00 – 17.00 Aseptic Processing of Sterile Products: Innovations, Regulatory Guidance and Compliance in a Practical World (E01)
Quality Risk Management: Focused, Practical Application (E02)
Data Integrity: How to Verify, Validate and Maintain (E03)
Inspection Readiness Workshop: From Site Preparation to Successful Execution (E04) (Cancelled)
Cleaning Validation Principles (T17)
Containment Fundamentals (T16) (Cancelled)
Wednesday
23 February
07.00 – 17.30 Registration Desk Open
07.30 – 09.00 Continental Breakfast in the Exhibit Hall
07.30 – 16.00 Exhibits Open
08.00 – 09.00 CPIP™ Introduction Workshop
09.00 – 17.00 Syringe Processing Workshop, 2nd Annual (E05)
Containment: A Risk-Based Approach (E06)
Pharmaceutical Inspections and Compliance - Current FDA Enforcement Trends (E07)
Energy Saving Projects – Case Studies and Tools for Saving Energy (E08)
Process Validation in Biotechnology Manufacturing (T32) Mouse icon indicates includes webinar
17.00 – 18.30 Networking Reception
Thursday
24 February
07.00 – 16.00 Registration Desk Open
07.00 – 08.00 Continental Breakfast
08.00 – 09.00 CPIP™ How-to Workshop
08.00 – 16.00 Syringe Processing Workshop, 2nd Annual (E05)
Containment: A Risk-Based Approach (E06)
Pharmaceutical Inspections and Compliance - Current FDA Enforcement Trends (E07)
Process Validation in Biotechnology Manufacturing (T32) Mouse icon indicates includes webinar
08.00 – 17.00 Energy Saving Projects – Case Studies and Tools for Saving Energy (E08)

Certified Pharmaceutical Industry Professional™ (CPIP™) certification program

Tampa Conference seminars may contain knowledge related to the Certified Pharmaceutical Industry Professional™ (CPIP™) certifcation program technical knowledge competency areas. Visit  www.ISPE-PCC.org for details. Completion of any of these seminars does not guarantee successful completion of the CPIP certification program exam.

See how conference seminars relate to CPIP Knowlege competency areas

Notice

ISPE leaders and speakers are leading professionals in their fields. However, in those rare circumstances where we find it necessary to make subsitutions, every possible effort is made to provide speakers with comparable qualifications. Agendas are subject to change without notice. Every precaution is taken to ensure accuracy, but ISPE cannot accept responsibility for the accuracy of information distributed or contained in these seminars or for any opinion expressed. Delegates’ names and addresses may be given as part of a list to other organizations for purposes related to the field of pharmaceutical manufacturing. If you do not wish to receive other related information, please notify ISPE.

Accreditation

ISPE provides continuing education units (ISPE CEUs). ISPE CEUs are nationally recognized units of attendance that identify those individuals continuing their education in their chosen field or profession. For the E06, Containment Technology Forum, CM Points for industrial hygienists have been applied for.


Computer Mouse Icon indicates included Webinar Some courses include a pre-recorded Webinar reviewing basic information so you can maximize your learning experience during the course. Access information will be provided via email one week prior to the start of the event.

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