Worldwide Regulatory expectations and guidance as led by FDA and the EU have stated that all Pharmaceutical Quality Systems should apply a QRM (Quality Risk Management) approach. Through interactive workshops, this course will explain and apply the science and risk-based approach to integrated....
Networking (ED)

Networking Opportunities

The 2017 ISPE Annual Meeting & Expo provides attendees with many opportunities to network with pharmaceutical industry professionals and regulators - unlike any other conference! Review the list below to identify which unique networking opportunities you'd like to register for today.

Venue (ED)

Hotel and Travel Details

Hotel

Marriott Marquis San Diego Marina
333 West Harbor Drive
San Diego, CA 92101 
+1-619-234-1500

Check in: 16.00
Check out: 12.00

Internet: Complimentary internet for ISPE attendees in guest rooms

Reservation Instructions

Room rate: $239 - City View
Room rate: $269 - Bay View

Through group exercises, this course on Quality by Design will delve into implementation and operation of an effective and efficient control strategy in manufacturing, which is a key element of process performance and product quality monitoring and continual improvement.
This training course on Pharmaceutical Technology Transfer identifies criteria for successful technology transfer and provides ‘how to’ examples which can be individually tailored, depending on the type and scope of transfer.
This training course examines current technology and provides scenario-based exercises for system troubleshooting and investigational events for process deviations, discusses quality management and GMP inspection preparation, and provides guidance on advanced asset lifecycle management strategy.
Explore the Programme (ED)

Explore the Programme


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This course will focus on using the logic diagram, how cross contamination control fits into the Quality System, how health-based limits are developed, setting cleaning validation limits, risk assessments for cross contamination and formulation a Quality Risk Management Plan.
This course is designed to help pharmaceutical manufacturing professionals chart a new course for innovation based on PAT. The course provides an overview to the tools and principles outlined in the FDA guidance, PAT - A Framework for Innovative Pharmaceutical Development, Manufacturing and Quality....
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