9th Annual Cleaning Validation

Venue: Park Hyatt at the Bellevue

Location: Philadelphia, Pennsylvania, United States

Event Date/Time: Jul 29, 2002 End Date/Time: Jul 31, 2002
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In its 9th year, the Cleaning Validation for Pharmaceutical and Biotech Manufacturers conference continues its strong tradition in providing the most effective strategies for implementing and executing a successful cleaning validation program. The research staff at IIR, together with our other advisory board members have redesigned the conference with an updated format and new short-courses, including one for clinical supplies manufacturers.
On Day One, we present two pre-conference shortcourses: Assembling the Proper Team to Conduct Cleaning Validation provides a detailed overview on defining personnel roles and organizing the team responsible for developing and executing a cleaning validation program. Our second short-course, Preparing a Thorough Master Plan to Ensure Successful Cleaning Validation is a step-by-step tutorial for developing a comprehensive cleaning validation master to be used as a virtual road map when conducting cleaning validation.
Day two kicks off the main conference, where the overall mission is to provide attendees with knowledge and strategies for successfully developing and implementing a fully compliant cleaning validation program that accurately tests equipment used in the manufacturing of pharmaceutical and biotech products. The first day of the main conference, July 29, 2002, features such companies as AstraZeneca, Cleaning Validation Technologies, McNeil Consumer Healthcare, Fluor Daniel and Steris Corporation and covers challenging topics including:

Interpret regulatory requirements for setting up a cleaning validation program
Set acceptable residue limits as part of the cleaning validation process
Develop accurate sampling and testing methods for measuring residues
Understand cleaning validation documentation requirements and preparing accurate records
Overcome cleaning validation change control challenges to ensure regulatory compliance and accurate documentation
Day three of the main conference features companies such as Watson Pharmaceuticals, Magellan Labs, Inc. and BioReliance addressing topics including:

Conducting a successful cleaning validation audit of contract manufacturers
Training and qualifying personnel to conduct cleaning validation and to reduce operator variability
Design and interpretation of viral and TSE cleaning studies for biopharmaceutical products
Also, for those of you involved in clinical supplies, don’t miss the newly added post-conference short course on Unique Hurdles for Conducting Cleaning Validation in the Clinical Manufacturing Environment. This short-course is specifically designed for Clinical Coordinators, Clinical Manufacturing Coordinators, Pilot Plant Managers and Clinical Pharmacy Managers and provides information on the distinctive challenges being faced when conducting cleaning validation when manufacturing clinical trial materials.
Meet your industry colleagues who share the same concerns and challenges in conducting cleaning validation. Join us and take back new insights guaranteed to give you a competitive edge. In addition to the hands-on experience you gain at the 9th Annual Cleaning Validation conference, you also receive a complete set of program documentation for future reference and a certificate of completion.