Upcoming Events
Date	Title	Location	Presenter
3/29/2012	PDA Southeast Spring Conference	Raleigh, NC	Booth
4/10/2012	ISPE-CASA Life Sciences Technology Show	Raleigh, NC	Booth
4/16-17/2012	PDA 2012 Annual Meeting	Phoenix, AZ	Booth
5/1-3/2012	Interphex 2012	New York, NY	Booth
6/24-27/2012	DIA 2012 Annual Meeting	Philadelphia, PA	Booth

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Past Events
Date	Title	Location	Presenter
6/23/2011	Vendor Qualification Audits for SaaS Suppliers Presentation DIA 2011 Annual Meeting	McCormick Place, Chicago, IL	Charles Lankford, Session Chair and Presenter
10/30/2010	LIMS Validation; Best Practices for Compliance at Implementation and Beyond	FDANews Webinar	Paul Krason
6/16/2010	Validating Clinical Applications in the Cloud	DIA 46th Annual Meeting Walter E. Washington Convention Center	Charles Lankford
6/25/2009	Tools and Techniques for Validating Open Source Systems	DIA 45th Annual Meeting San Diego Convention Center	Wyetta Palmby
4/22/2009	Clean-In-Place (CIP) & Sterilize-In-Place (SIP) Systems in the Biopharmaceutical Industry, Improving Process Reliability through Computerization Presentation	2009 PDA Annual Meeting	Charles Lankford
3/30/2009	Cleaning Validation Fundamentals The "What,Why, and When" of Cleaning Validation	Hilton Raleigh-Durham at Research Triangle Park	TBD
10/28/2008	Poster: Implementing and Maintaining an Effective Quality Management System Explaining the keys to a successful QMS and the basics of implementaion and maintenance.	ISPE 08 Annual Meeting	Wyetta Palmby Charles Lanford
10/28/2008	Poster: Thermal Validation Systems Covers the topic of choosing the right Thermal Validation System, NIST traceability standards, 21 CFR Part 11 compliance, temperature controlled environments, common uses for Thermal Validation, and common manufacturers	ISPE 08 Annual Meeting	Aqueelah Patterson Charles Lankford
10/21/2008	Validation of EDC DIA Data Driven Drug Deveopment Conference, Ljubjana, Slovenia	Ljubljana, Slovenia	Charles Lankford
9/8/2008	Computerized Systems in Clinical Research:Current Quality and Data Integrity Concepts DIA conference to develop a useful reference for computerized systems in clinical research	DIA Headquarters, Horsham, PA	Matthew Tedder, contributor to Chapter 17
7/22/2008	RNA Therapeutics Bringing the Future of Biological and Medical Innovation to Today	Boston, MA	Barry Crawford, Ph.D.
4/14/2008	PDA Annual Meeting Poster – “A Risk Based Approach To Validation”	Colorado Springs, CO	Brian Yancey
3/26/2008	Fundamentals of Cleaning Validation Interphex Conference	Philadelphia PA	Kris Kelly
3/17/2008	23rd Annual DIA Data Management in Transition: Putting the “e” in Data Management Validating Electronic Data Capture Systems	Washington, DC	Wyetta Palmby
3/8/2007	Qualification of a Mass Spectrometer System: A Case Study	Philadelphia, PA	Chris Haskett
10/29/2006	PDA Microbiology Forum	Bethesda, MD	Nancy Tomoney
5/17/2006	Validation of Bioreactors in a Biological Production Facility To comply with regulatory requirements a company must validate bioreactors as well as the steps used to manufacture biological products	Web Seminar	Charles Lankford & Brett Yates
4/24/2006	PDA National Meeting Designing and Using Formal Annual Environmental Monitoring Reports to Discuss Annual Performance of Utility Systems	Anaheim, CA	Nancy E. Tomoney
4/24/2006	PDA Annual Meeting Validation of Bioreactors in a Biological Manufacturing Facility	Anaheim, CA	Charles Lankford
3/31/2006	IVT The When, Where, Why and How Often of Filter Validation	San Francisco, CA	Nancy E. Tomoney
3/29/2006	IVT Validation of Analytical Laboratory Equipment and Support Systems	San Francisco, CA	Nancy E. Tomoney
3/28/2006	IVT Aseptic Processing & Sterile Processes	San Francisco, CA	Nancy E. Tomoney
3/22/2006	DIA - Follow-up to the Red Apple Conference Computerized Systems for Nonclinical Safety Assessment:: Current Concepts and Quality Assurance	Horsham, PA	Charles Lankford
3/21/2006	Interphex Techniques for Running a Lean Commissioning / Validation Project	New York City, NY	Charles Lankford
3/1/2006	PDA Metro Chapter Meeting Qualification of Pharmaceutical Water Systems	Clark, NJ	Nancy E. Tomoney
6/27/2005	IPQC Analytical Instrument Qualification	Philadelphia, PA	Nancy Tomoney
3/15/2005	Lab Equipment Validation and Qualification Strategies for validation and qualification of lab instruments and computer systems to ensure optimal compliance.	Brussels, Belgium	Charles Lankford
3/7/2005	Lab Equipment Validation and Qualification Strategies for validation and qualification of lab instruments and computer systems to ensure optimal compliance.	Philadelphia, PA	Charles Lankford
2/1/2005	IT Infrastructure Qualification Conference Creating and Maintaining a Compliant Network Infrastructure in a Small-Mid Cap Company	Las Vegas, NV	Matt Tedder
12/4/2004	Barnett International Identifying Regulatory Requirements and Developing a Project Plan to Implement a Successful Environmental Monitoring Program	Philadelphia, PA	Nancy Tomoney
11/18/2004	IVT Developing and Executing Microbial Cleaning Validation Protocols to Comply with FDA Requirements.	Amsterdam, The Netherlands	Nancy Tomoney
11/16/2004	IVT Cleaning Validation Mistakes: How Not to Perform Cleaning Validation: A Review of Regulatory Citations and Solutions to Avoid Making the Same Mistake.	Amsterdam, The Netherlands	Nancy Tomoney
9/13/2004	Barnett International Successfully Validating Compendial Water Systems- Establishing Microbial Control	Philadelphia, PA	Nancy Tomoney
6/16/2004	DIA 40th Annual Meeting Validating Clinical Data Systems	Washington, DC	Charles Lankford
6/10/2004	PDA Audio Conference FDA's New Barcode Requirement When, Where and How to Comply	Audio Conference	Hal Sanborn
5/17/2004	Center for Professional Advancement Computer Validation (Manufacturing)	Boca Raton, FL
3/15/2004	Center for Professional Advancement GLPs and Part 11	San Francisco, CA
3/11/2004	DIA 9th Annual Computer Validation Conference: Computer Automated Testing Tools Regulatory and Validation Impacts	Arlington, VA	Matthew Tedder
2/10/2004	Center for Professional Advancement GLPs and Part 11	Boca Raton, FL
1/12/2004	Center for Professional Advancement Computer Validation (R&D)	San Francisco, CA
11/11/2003	Barnett International Validation / Risk and Maintenance System	Brussels, Belgium
11/11/2003	2003 PDA Annual Meeting Computer Automated Testing Tools Regulatory and Validation Impacts	Atlanta, GA	Matthew Tedder
10/27/2003	Center for Professional Advancement Topic Computer Validation (R&D)	New Brunswick, NJ
8/28/2003	The SMi Group Validation of Clinical	London, England UK	Jeffery Taylor
8/1/2003	Barnett International Validation of Building Management Systems	Philadelphia, PA	Chris Haskett
6/24/2003	Barnett International Developing Concise Software Validation Master Plans	Philadelphia, PA	Jeffery Taylor
3/17/2003	Barnett International Understanding 21 CFR Part 11 Remediation for Legacy Systems	Philadelphia, PA	Matthew Tedder