Register Now for the Institute of Validation Technology's
Validation and cGXP Compliance Workshop Series
July 12-15, 2005 San Juan, Puerto Rico
Wyndham El San Juan Hotel and Casino

Keynote Presentation: FDA Review of Current Good Manufacturing Practices (cGMPs): Manufacturing Process Validation and Supporting Systems Qualification
Arlene M. Badillo, Drug Specialist Investigator, FDA San Juan District Office

Conference Details: Download Event Brochure & Registration Form (pdf)

Choose From 32 Interactive Workshops Sessions and Including:

Process FMEA A Risk Analysis Tool for Process Validation
Lessons Learned in Software Quality Analysis
Using Statistics for an Effective Process Validation
Developing and Utilizing an Effective Validation Master Plan
Auditing Validation Programs
Equipment Qualification Case Study
Validation Training 101
Establishing a Change Control Culture
Writing Validation Protocols
Current Issues in Cleaning Validation
FDA Systems-Based Inspections
Laboratory Instrument Qualification
Extending Your Quality System to Your Vendor
Hear from 18 Pharmaceutical/Biotechnology Companies, FDA and Allied Companies, Including:

Alcon Laboratories
Avarent
BBI Biotech Research
Diosynth
U.S. FDA
MannKind BioPharmaceuticals
McNeil Consumer Healthcare
Quintiles
Validation Technologies
Create-Your-Own Conference:
This unprecedented industry event offers the opportunity to attend single workshops or the entire program. Attendees can design their own conference by choosing from various 90-minute, half-day, and interactive sessions.


To Register:


Download Event Brochure & Registration Form (pdf)

or Phone: 218-723-9130, U.S. Only: 888-524-9922
Fax: 218-723-9308
Email: registration@ivthome.com

For Speaking Opportunities Contact:

Jessica Hudson
jhudson@advanstar.com
954-567-9402

For Exibitor or Sponsorship Opportunities: please call 561-790-2025. View all IVT Conference Events