Home Suppliers News Events Library Surveys/Polls Software Downloads Job Board Bid Opportunities
 ", true); $zoneAdLeft .= GetZoneSnippet(30, "
 
", true); $zoneAdLeft .= GetZoneSnippet(31, "
 
", true); $zoneAdLeft .= GetZoneSnippet(32, "
 
", true); $zoneAdLeft .= GetZoneSnippet(33, "
 
", true); $zoneAdLeft .= GetZoneSnippet(34, "
 
", true); $zoneAdLeft .= GetZoneSnippet(35, "
 
", true); $zoneAdLeft .= GetZoneSnippet(36, "
 
", true); $zoneAdLeft .= GetZoneSnippet(37, "
 
", true); $zoneAdLeft .= GetZoneSnippet(38, "
 
", true); echo($zoneAdLeft); ?>
Events

E-mail this pageEmail a link to this Page

 

 LIMSfinder.com "Events"

...provides a listing of events by event date.

View All Events     View Events by Category


List of Past Events for Compliance
Date Event Location Category
10/02/2007
The Institute of Validation Technology Lab Week

The Only Conference Featuring the Three Hottest Lab Topics in One Fantastic Event: Method Validation FDA/USP Guidances, Statistics, Analytical Method Transfer, Test Method Validation, Validation of Compendial Procedures, Cleaning Methods for Potent Compounds, LC Method Development, and more.

Posted by: limsfinder - 0 comments   
Read and Post Comments
San Diego, California Compliance
08/30/2007
"Auditing/Gap Analysis: QSIT Auditing for Regulatory Compliance, including Part 11, Part 211 and Part 820" - Live Web Seminar

The FDA implemented the Quality System Inspection Technique (QSIT) as a standard approach for FDA investigators. While field investigations are traditionally approached from a “root cause analysis” of observed problems, QSIT uses a "top down" approach making management of the quality system the central theme.
Posted by: limsfinder - 0 comments   
Read and Post Comments
Live Web Seminar Compliance
07/25/2007
The Essentials of Effectively Managing QA/QC Departments

Live Web Seminar - Wednesday, July 25, 2007
Posted by: limsfinder - 0 comments   
Read and Post Comments
Live Web Seminar Compliance
06/04/2007
Q9 QUALITY RISK MANAGEMENT conference in San Diego!

SWE Enterprises, Inc. invites you to attend the Strategies to Effectively Apply Q9 QUALITY RISK MANAGEMENT in the FDA Regulated Industry conference. This Educational Conference event will provide in-depth coverage on Tools, Techniques and Experiences in Utilizing Q9 Quality Risk Management for Enhanced Efficiencies and Regulatory Compliance. It will be held at the La Jolla Marriott in San Diego, CA on June 4-5, 2007!

Posted by: limsfinder - 0 comments   
Read and Post Comments
San Diego, California Compliance
05/17/2007
ADVANCED COMPUTER SYSTEM VALIDATION Conference in Boston on May 17-18, 2007

SWE Enterprises, Inc. invites you to attend the Third Annual ADVANCED COMPUTER SYSTEM VALIDATION Conference for the Pharmaceutical, Biotech and Medical Device Industries. The conference will provide in-depth coverage practical approaches to utilize of risk management, COTS, GAMP and other tools and techniques for more effective and efficient Computer System Validation without jeopardizing Regulatory Compliance. It will be held at the Tremont Marriott in Boston, MA on May 17-18, 2007!

Posted by: limsfinder - 0 comments   
Read and Post Comments
Boston, Massachusetts Compliance
05/16/2007
4th Annual International Meeting on Automated Compliance Systems

The IMACS Organizing Committee is pleased to announce the preliminary agenda for the 4th annual IMACS conference on May 16-17 in Princeton, NJ. IMACS was developed to provide a forum to detail IT-based compliance and productivity solutions for pharmaceutical, biotechnology, medical device, and contract laboratories in Development and QC/QA.

Posted by: limsfinder - 0 comments   
Read and Post Comments
Princeton, New Jersey Compliance
11/08/2006
Seventh Annual Pharmaceutical Regulatory and Compliance Congress

Seventh Annual Pharmaceutical Regulatory and Compliance Congress

Posted by: limsfinder - 0 comments   
Read and Post Comments
Washington, DC Compliance
10/23/2006
Clinical Trials in Canada

New legal obligations and compliance standards are now being imposed for every significant aspect of clinical trials in Canada. Be prepared… Register NOW!
Posted by: limsfinder - 0 comments   
Read and Post Comments
Toronto, Canada Compliance
09/14/2006
Webinar: cGMP Informatics – A Three Layer Infrastructure in Quality Operations with ERP, LIMS, and ELN

The web briefing is based on a report from an automated compliance industry conference where Eli Lilly, BMS, AstraZeneca, GSK and others outlined a quality lab operations structure for 21st century cGMP workflow, instrument integration and data management.
Posted by: limsfinder - 0 comments   
Read and Post Comments
Webinar Compliance
08/22/2006
The Second Annual FDA Regulatory and Compliance Symposium

Managing Risks — From Pipeline to Patient
Posted by: limsfinder - 0 comments   
Read and Post Comments
Cambridge, Massachusetts Compliance
07/20/2006
3rd Laborarory Equipment Qualification and Systems Validation Conference

For the Pharmaceutical and Biotech Industries. Practical Approaches to Understanding Current FDA Expectations for Regulatory Compliance
Posted by: limsfinder - 0 comments   
Read and Post Comments
LaJolla, California Compliance
07/20/2006
Impurity Testing in Drug Substances and Products Conference

Understanding the Requirements for Regulatory Compliances, Safety Thresholds and Methods to Achieve Both
Posted by: limsfinder - 0 comments   
Read and Post Comments
La Jolla, California Compliance
05/17/2006
IMACS 2006, International Meeting on Automated Compliance Systems for the Life Science Industry

IMACS (International Meeting on Automated Compliance Systems), is the definitive conference on IT-based compliance and productivity solutions. The life science industry is challenged with reducing costs and improving productivity throughout the drug development and production process. IMACS is dedicated to providing an information exchange for enabling technologies designed to meet those challenges.

Posted by: limsfinder - 0 comments   
Read and Post Comments
Princeton, NJ Compliance
02/27/2006
Process Validation of Biologicals

Analyzing Validation Activities to Mitigate Risk and Incorporate New Technologies
Posted by: limsfinder - 0 comments   
Read and Post Comments
Carlsbad, California Compliance
01/30/2006
Cold Chain Management and Distribution Conference

"Effective and Compliant Cold Chain Management and Distribution in the Regulated Industry"
Posted by: limsfinder - 0 comments   
Read and Post Comments
San Diego, California Compliance
12/13/2005
Structured Product Labeling

Four Strategies to Comply With the New SPL Mandate

Posted by: limsfinder - 0 comments   
Read and Post Comments
AUDIOCONFERENCE Compliance
11/21/2005
9th Annual European Scientific and Regulatory Affairs

Posted by: limsfinder - 0 comments   
Read and Post Comments
Paris, France Compliance
08/24/2005
FDA Regulatory and Compliance Symposium

Managing Risks — From Pipeline to Patient
Posted by: limsfinder - 0 comments   
Read and Post Comments
Cambridge, Massachusetts Compliance
07/25/2005
Design and Implementation of Environmental Monitoring in the FDA Regulated Industry"

"Practical Approaches to Design, Implementation and Trending of Environmental Conditions to Achieve FDA Compliance" AND "Exploring Current Strategies in Research, Development Production and Litigation in Polymorphism and Crystallization in the Regulated Industry"
Posted by: limsfinder - 0 comments   
Read and Post Comments
San Diego, California Compliance
06/28/2005
Lab Compliance & Analytical Equipment Qualification

By attending PharmaIQ's Lab Compliance & Analytical Equipment Qualification conference, you will learn how leading companies have implemented best practices and successful methodologies to overcome compliance challenges.
Posted by: limsfinder - 0 comments   
Read and Post Comments
Philadelphia, Pennsylvania Compliance
05/16/2005
9th Annual eSubmissions: Transitioning to eCTDs - Regulatory, Resource and Technical Challenges

Join the Institute for International Research for our ninth annual eSubmissions conference, where you will learn how to overcome regulatory, resource and technical challenges as you transition to eCTDs.
Posted by: limsfinder - 0 comments   
Read and Post Comments
Arlington, Virginia Compliance
05/02/2005
Laboratory Instrument Qualification and Validation Systems

The Laboratory Compliance Conference of the Year - "Understanding Current FDA Expectations and Regulatory Compliance for Laboratory Instrument Qualification and Systems Validation"

Posted by: limsfinder - 0 comments   
Read and Post Comments
East Hanover Marriott, Whippany, New Jersey Compliance
03/21/2005
CHI's - Quantitative PCR

Changes in gene expression underlie many biological phenomena. Researchers, using microarrays or RNAi for mapping cellular pathways, prioritizing suitable targets for pharmaceutical intervention or diagnostics, determining toxicology or prognostics (disease progression), will find this meeting useful for developing qPCR as their validation tool of choice.
Posted by: limsfinder - 0 comments   
Read and Post Comments
La Jolla, California Compliance
03/07/2005
2005 Pharma IT Compliance Week

The Regulatory Compliance Workshop Group proudly presents Pharma Industry’s Premier Training Event - 2005 Pharma IT Compliance Week - “The FDA and European Regulators’ Latest Thinking for those working to GCP, GMP and GLP”
Posted by: limsfinder - 0 comments   
Read and Post Comments
San Juan, Puerto Rico Compliance
02/14/2005
Process Validation for Biological Production

A practical guide for gaining product approval
Posted by: limsfinder - 0 comments   
Read and Post Comments
Geneva, Switzerland Compliance
12/06/2004
Advanced Computer System Validation Conference

"Strategies for Meeting Current FDA Expectations for Computer Systems
Posted by: limsfinder - 0 comments   
Read and Post Comments
San Diego, California Compliance
11/15/2004
2004 U.S. Pharma IT Compliance Workshops

The Regulatory Compliance Workshop Group proudly presents USA’s Premier Training Event - 2004 U.S. Pharma IT Compliance Workshops “The FDA and European Regulators’ Latest Thinking for those working to GCP, GMP and GLP”
Posted by: limsfinder - 0 comments   
Read and Post Comments
Philadelphia, Pennsylvania USA Compliance
10/18/2004
The Laboratory Compliance Conference of the Year

"Understanding Current FDA Expectations and Regulatory Compliance for Laboratory Instrument Qualification and Systems Validation"
Posted by: limsfinder - 0 comments   
Read and Post Comments
La Jolla Marriott * San Diego, CA Compliance
09/27/2004
2004 European Pharma IT Compliance Workshops - Regulatory Compliance Workshop Group

Five 1-day workshops explaining how to satisfy the FDA and European regulators.
Posted by: RCWG - 0 comments   
Read and Post Comments
London, UK Compliance
07/22/2004
IT Infrastructure Qualification and Systems Validation

Ensuring FDA Compliance for Network Configuration Management, Validation and Change Control
Posted by: limsfinder - 2 comments   
Read and Post Comments
San Diego, CA Compliance
  

Copyright - W3Markets, Inc.

  Legal Notices & Terms of Use