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Event The Latest Developments in FMLA and ADA - Webinar By TrainHR
Begins January 18, 2012
City Wilmington
Country USA

Event The Fallacies Of Performance Appraisals And How To Overcome Them - Webinar By TrainHR
Begins January 11, 2012
City Wilmington
Country USA

Event Reference and Background Checking to Assure the Right Hires - Webinar By TrainHR
Begins December 20, 2011
City Wilmington
Country USA

Event Payroll Best Practices: Proper Handling of Multistate Taxation - Webinar By TrainHR
Begins December 14, 2011
City Wilmington
Country USA

Event Virtual Teams: How to Sustain High Performing Teams in the Virtual Workplace - Webinar By TrainHR
Begins December 13, 2011
City Wilmington
Country USA

Event Assessments: The good, The bad, and the Ugly - Webinar By TrainHR
Begins November 15, 2011
City Wilmington
Country USA

Event Performance Management: The Key to the Castle - Webinar By TrainHR
Begins November 1, 2011
City Wilmington
Country USA

Event Calculating Overtime Correctly - Webinar By TrainHR
Begins October 27, 2011
City Wilmington
Country USA

Event Workplace Violence Prevention - Webinar By TrainHR
Begins October 20, 2011
City Wilmington
Country USA

Event Human Capital, Organizational Structure and Human Resources - Webinar By TrainHR
Begins October 18, 2011
City Wilmington
Country USA

Event Preventing Repetitive Motion Injury Through Cost Saving Ergonomics And Workers Compensation Management Strategies - Webinar By TrainHR
Begins October 11, 2011
City Wilmington
Country USA

Event Winning Networking Strategies - Webinar By TrainHR
Begins October 6, 2011
City Wilmington
Country USA

Event Managing Employee Behavior Problems - Webinar By TrainHR
Begins October 4, 2011
City Wilmington
Country USA

Event Documenting Payroll Procedures - Webinar By TrainHR
Begins September 29, 2011
City Wilmington
Country USA

Event Legal and Effective Hiring and Interviewing - Webinar By TrainHR
Begins September 29, 2011
City Wilmington
Country USA

Event Motivating Employees for Winning Performance - Webinar By TrainHR
Begins September 28, 2011
City Wilmington
Country USA

Event HR Metrics for the Human Resource Executive - Webinar By TrainHR
Begins September 20, 2011
City Wilmington
Country USA

Event W2s 1099s Independent Contractors? Protect Yourself with Proper Classification - Webinar By TrainHR
Begins August 18, 2011
City Wilmington
Country USA

Event The Law and Psychology of Mental Health Issues at Work: Substance Abuse, Depression and the Bermuda Triangle of the ADA, the FMLA and Workers Comp -
Begins August 17, 2011
City Wilmington
Country USA

Event Valuing and Understanding Diversity in the Workplace Today - By TrainHR
Begins August 9, 2011
City Wilmington
Country USA

Event Creation and management of a Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Co
Begins August 9, 2011
City Wilmington
Country USA

Event Understanding At-Will Employment and Using That Knowledge to Manage Better - Webinar By TrainHR
Begins August 4, 2011
City Wilmington
Country USA

Event Controlling Workers Comp Injuries As Your Workforce Ages - Webinar By TrainHR
Begins August 3, 2011
City Wilmington
Country USA

Event Coaching and Mentoring for High Performance - Webinar By TrainHR
Begins August 2, 2011
City Wilmington
Country USA

Event Creation and configuration of a Equipment, Facilities, and Preventive Maintenance System utilizing the principles of Lean Documents and Lean Configura
Begins July 26, 2011
City Wilmington
Country USA

Event Document Retention and Destruction - Webinar By TrainHR
Begins July 14, 2011
City Wilmington
Country USA

Event Auditing and Administrating Human Resources Policies and Practices - By TrainHR
Begins July 14, 2011
City Wilmington
Country USA

Event Auditing and Administrating Human Resources Policies and Practices - By TrainHR
Begins July 7, 2011
City Wilmington
Country USA

Event Document Retention and Destruction - Webinar By TrainHR
Begins July 7, 2011
City Wilmington
Country USA

Event DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
Begins June 29, 2011
City Wilmington
Country USA

Event HIPAA Enforcement and Compliance Audits: What the auditors want and how to be ready before they call - Webinar By GlobalCompliancePanel
Begins June 23, 2011
City Wilmington
Country USA

Event Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
Begins June 17, 2011
City Wilmington
Country USA

Event How to Survive a DEA Audit - Webinar By GlobalCompliancePanel
Begins June 14, 2011
City Wilmington
Country USA

Event Develop and Execute the Company Software V&V Program - Webinar By GlobalCompliancePanel
Begins June 8, 2011
City Wilmington
Country USA

Event Product Recalls - Planning and Conducting Food Recall - Webinar By GlobalCompliancePanel
Begins June 8, 2011
City Wilmington
Country USA

Event Effective Risk Based Approach to Auditing and Qualifying Suppliers and Vendors - Webinar By GlobalCompliancePanel
Begins June 8, 2011
City Wilmington
Country USA

Event HIPAA Security Policies and Procedures: Making them useful and relevant as well as compliant - Webinar By GlobalCompliancePanel
Begins June 7, 2011
City Wilmington
Country USA

Event Pharmaceutical and Medical Device Validation Guidances - Similarities and Differences - Webinar By GlobalCompliancePanel
Begins May 26, 2011
City Wilmington
Country USA

Event Root Cause Analysis - The Heart of a Successful CAPA Program - Webinar By GlobalCompliancePanel
Begins May 25, 2011
City Wilmington
Country USA

Event FDAs Update on Medical Device Labeling Changes - Webinar By GlobalCompliancePanel
Begins May 24, 2011
City Wilmington
Country USA

Event GMP Expectations for Products Used in Early Phase IND Studies - Webinar By GlobalCompliancePanel
Begins May 24, 2011
City Wilmington
Country USA

Event Information Security and Payment Card Rules: Protecting Patient Payment Data and Complying with PCI - Webinar By GlobalCompliancePanel
Begins May 24, 2011
City Wilmington
Country USA

Event Complaint Handling in Compliance with FDA and ISO Regulations - Webinar By GlobalCompliancePanel
Begins May 19, 2011
City Wilmington
Country USA

Event Recalls & Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel
Begins May 19, 2011
City Wilmington
Country USA

Event Test Method Validation - The Characteristics - Webinar By GlobalCompliancePanel
Begins May 19, 2011
City Wilmington
Country USA

Event Requirements of the Master Production Record - Webinar By GlobalCompliancePanel
Begins May 18, 2011
City Wilmington
Country USA

Event Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel
Begins May 18, 2011
City Wilmington
Country USA

Event The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - barriers and solution - Webinar By GlobalCompliancePanel
Begins May 17, 2011
City Wilmington
Country USA

Event Conducting Successful Product Complaint Investigations - Webinar By GlobalCompliancePanel
Begins May 12, 2011
City Wilmington
Country USA

Event Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel
Begins May 12, 2011
City Wilmington
Country USA

Event Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained
Begins May 11, 2011
City Wilmington
Country USA

Event 21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection - Webinar By GlobalCompliancePanel
Begins May 11, 2011
City Wilmington
Country USA

Event Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel
Begins May 11, 2011
City Wilmington
Country USA

Event Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel
Begins May 10, 2011
City Wilmington
Country USA

Event FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP
Begins May 10, 2011
City Wilmington
Country USA

Event Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel
Begins May 5, 2011
City Wilmington
Country USA

Event Information Security Risk Analysis: Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePanel
Begins May 5, 2011
City Wilmington
Country USA

Event FDAs New Enforcement of 21 CFR Part 11 - Webinar By GlobalCompliancePanel
Begins May 4, 2011
City Wilmington
Country USA

Event Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel
Begins May 4, 2011
City Wilmington
Country USA

Event Good Documentation Practices for GMP Operations - Webinar By GlobalCompliancePanel
Begins May 3, 2011
City Wilmington
Country USA

Event The Most Common Problems in FDA Software Validation & Verification - Webinar By GlobalCompliancePanel
Begins May 3, 2011
City Wilmington
Country USA

Event FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
Begins May 3, 2011
City Wilmington
Country USA

Event Gowning Systems Used in Cleanrooms & Controlled Environments - Webinar By GlobalCompliancePanel
Begins April 28, 2011
City Wilmington
Country USA

Event Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel
Begins April 28, 2011
City Wilmington
Country USA

Event How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel
Begins April 27, 2011
City Wilmington
Country USA

Event Webinar on Cloud Computing / SaaS - Webinar By GlobalCompliancePanel
Begins April 21, 2011
City Wilmington
Country USA

Event Overall Residual Risk Evaluation - Webinar By GlobalCompliancePanel
Begins April 20, 2011
City Wilmington
Country USA

Event Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel
Begins April 19, 2011
City Wilmington
Country USA

Event Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel
Begins April 14, 2011
City Wilmington
Country USA

Event Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDAs Framework of Acceptable Practices - Webinar By GCPanel
Begins April 13, 2011
City Wilmington
Country USA

Event Facilities Cleaning in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
Begins April 13, 2011
City Wilmington
Country USA

Event Understanding Attribute Acceptance Sampling including Z1.4 and c=0 Plans - Webinar By GlobalCompliancePanel
Begins April 13, 2011
City Wilmington
Country USA

Event Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel
Begins April 12, 2011
City Wilmington
Country USA

Event HIPAA Business Associates: How the regulations have changed, and what you need to do for compliance now - Webinar By GCPanel
Begins April 7, 2011
City Wilmington
Country USA

Event Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
Begins April 7, 2011
City Wilmington
Country USA

Event Change Control -- Your Companys GMP Weak Point - Webinar By GlobalCompliancePanel
Begins April 6, 2011
City Wilmington
Country USA

Event The Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel
Begins April 6, 2011
City Wilmington
Country USA

Event Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel
Begins April 5, 2011
City Wilmington
Country USA

Event Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel
Begins April 5, 2011
City Wilmington
Country USA

Event A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - Webinar By GCPanel
Begins March 30, 2011
City Wilmington
Country USA

Event Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel
Begins March 29, 2011
City Wilmington
Country USA

Event The Pharmaceutical Quality System - Webinar By GlobalCompliancePanel
Begins March 29, 2011
City Wilmington
Country USA

Event March 26th Battleship North Carolina with Loyd Auerbach - Andy Andrews - Ashley Godwin - Susan Slaughter GHI - Ghost Hunters International - Plus spec
Begins March 26, 2011
City Wilmington
Country USA

Event Validation of Existing/Legacy Computer Systems for FDA/EU Compliance - Webinar By GlobalCompliancePanel
Begins March 23, 2011
City Wilmington
Country USA

Event Medical Device Recalls: How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel
Begins March 22, 2011
City Wilmington
Country USA

Event Documentation for IEC 60601-1 3rd Edition Compliance - Webinar By GlobalCompliancePanel
Begins March 22, 2011
City Wilmington
Country USA

Event Introduction to Contamination Control Master Plans - Webinar by GlobalCompliancePanel
Begins March 17, 2011
City Wilmington
Country USA

Event Regulatory Complaint Handling, Vigilance & Recalls - Webinar By GlobalCompliancePanel
Begins March 17, 2011
City Wilmington
Country USA

Event Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel
Begins March 15, 2011
City Wilmington
Country USA

Event HIPAA Breach Notification: What to do to prevent breaches, and what to do when they happen to you - Webinar By GCPanel
Begins March 15, 2011
City Wilmington
Country USA

Event Effective Corrective and Preventive Actions (CAPA): 10 Steps to Success - GlobalCompliancePanel Virtual Seminar - Webinar By GlobalCompliancePanel
Begins March 10, 2011
City Wilmington
Country USA

Event Developing the Risk Management Plan - Webinar By GlobalCompliancePanel
Begins March 10, 2011
City Wilmington
Country USA

Event Tougher U.S. FDA cGMP Compliance Audits - When Youre Not Ready - Webinar by GlobalCompliancePanel
Begins March 9, 2011
City Wilmington
Country USA

Event Statistical Concepts of Process Validation - Webinar By GlobalCompliancePanel
Begins March 9, 2011
City Wilmington
Country USA

Event Chemical Control for Food Manufacturers: Ingredient, Cleaning and Hazardous Materials - Webinar By GlobalCompliancePanel
Begins March 8, 2011
City Wilmington
Country USA

Event Process Validation: current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel
Begins March 8, 2011
City Wilmington
Country USA

Event Purchasing and Supplier Controls in the Medical Device Industry - Webinar By GlobalCompliancePanel
Begins March 3, 2011
City Wilmington
Country USA

Event Why is CAPA so often cited in medical device inspections - Webinar By GlobalCompliancePanel
Begins February 24, 2011
City Wilmington
Country USA

Event 21 CFR Part 11 - Compliance for Electronic Records and Signatures - Webinar By GlobalCompliancePanel
Begins February 24, 2011
City Wilmington
Country USA

Event Cleanroom & HEPA Filter Testing & Certification: An Owners Guide - Webinar by GlobalCompliancePanel
Begins February 24, 2011
City Wilmington
Country USA

Event Medical Device Changes and The 510(k) - Webinar By GlobalCompliancePanel
Begins February 23, 2011
City Wilmington
Country USA

Event Practical Laboratory Statistics - Webinar by GlobalCompliancePanel
Begins February 23, 2011
City Wilmington
Country USA

Event International Financial Reporting Standards: The Basics - Webinar by GlobalCompliancePanel
Begins February 23, 2011
City Wilmington
Country USA

Event Complying with HIPAA Security Rules: Whats in the rules and how you can most easily prepare for compliance - Webinar By GlobalCompliancePanel
Begins February 22, 2011
City Wilmington
Country USA

Event Using Foreign Trial Data in Your NDA Approval Process - Webinar By GlobalCompliancePanel
Begins February 22, 2011
City Wilmington
Country USA

Event Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - Webinar By GlobalCompliancePanel
Begins February 22, 2011
City Wilmington
Country USA

Event Electronic Raw Data in Regulated Environments - Definition, Recording and Archiving - Webinar By GlobalCompliancePanel
Begins February 17, 2011
City Wilmington
Country USA

Event Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
Begins February 17, 2011
City Wilmington
Country USA

Event 21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar - Webinar By GlobalCompliancePanel
Begins February 17, 2011
City Wilmington
Country USA

Event Medical Device Reporting Regulations and Violations - Webinar By GlobalCompliancePanel
Begins February 16, 2011
City Wilmington
Country USA

Event Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel
Begins February 16, 2011
City Wilmington
Country USA

Event Controlled Substances and the Pharmacist - Webinar By GlobalCompliancePanel
Begins February 15, 2011
City Wilmington
Country USA

Event Operational Risk Management: Ensuring Safety for Food Systems - Webinar By GlobalCompliancePanel
Begins February 10, 2011
City Wilmington
Country USA

Event Internal Audits: Maintaining your Quality Systems at the Ready - Webinar By GlobalCompliancePanel
Begins February 10, 2011
City Wilmington
Country USA

Event Food Safety Management Systems - ISO 22000:2005 - Webinar By GlobalCompliancePanel
Begins February 10, 2011
City Wilmington
Country USA

Event Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel
Begins February 9, 2011
City Wilmington
Country USA

Event Utilizing Good Requirements as a Foundation for the Effective Validation of PDMA-related Computerized Systems - Webinar By GlobalCompliancePanel
Begins February 9, 2011
City Wilmington
Country USA

Event Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel
Begins February 9, 2011
City Wilmington
Country USA

Event Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel
Begins February 8, 2011
City Wilmington
Country USA

Event Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webianr By GlobalCompliancePanel
Begins February 8, 2011
City Wilmington
Country USA

Event Hazard Analysis vs. FMECA – Differences and Commonalities - Webinar By GlobalCompliancePanel
Begins February 8, 2011
City Wilmington
Country USA

Event How to Prepare and Submit a Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
Begins February 3, 2011
City Wilmington
Country USA

Event Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel
Begins February 3, 2011
City Wilmington
Country USA

Event Legal Risks in Social Media for Healthcare Providers - Webinar By GlobalCompliancePanel
Begins February 3, 2011
City Wilmington
Country USA

Event Reprocessing REUSABLE Medical Devices-Cleaning & Labeling Requirements - Webinar By GlobalCompliancePanel
Begins February 2, 2011
City Wilmington
Country USA

Event New Changes to HIPAA: The latest changes in the regulations and what they mean to you - Webinar By GlobalCompliancePanel
Begins February 1, 2011
City Wilmington
Country USA

Event Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained
Begins February 1, 2011
City Wilmington
Country USA

Event Webinar on Pharmacovigilance Audit - Webinar By GlobalCompliancePanel
Begins January 27, 2011
City Wilmington
Country USA

Event Excel Spreadsheets - Develop and Validate to Eliminate 483s - Webinar By GlobalCompliancePanel
Begins January 27, 2011
City Wilmington
Country USA

Event Defining and Managing Protocol Deviation/Violation/Exception - Webinar By GlobalCompliancePanel
Begins January 26, 2011
City Wilmington
Country USA

Event Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
Begins January 26, 2011
City Wilmington
Country USA

Event Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel
Begins January 25, 2011
City Wilmington
Country USA

Event Understanding and Preparing for FDAs New Part 11 Inspection Program - Webinar By GlobalCompliancePanel
Begins January 25, 2011
City Wilmington
Country USA

Event Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel
Begins January 20, 2011
City Wilmington
Country USA

Event Preventive and Corrective Maintenance: Protect your assets, Protect your consumers - Webinar By GlobalCompliancePanel
Begins January 20, 2011
City Wilmington
Country USA

Event Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel
Begins January 20, 2011
City Wilmington
Country USA

Event Medical Device Tracking: Latest FDA Update and Expectations - Webinar By GlobalCompliancePanel
Begins January 19, 2011
City Wilmington
Country USA

Event Responding to FDA 483s to avoid warning letters - Webinar By GlobalCompliancePanel
Begins January 19, 2011
City Wilmington
Country USA

Event Statistical Sampling Plans for Audits - Webinar By GlobalCompliancePanel
Begins January 18, 2011
City Wilmington
Country USA

Event How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By GlobalCompliancePanel
Begins January 18, 2011
City Wilmington
Country USA

Event Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompliancePanel
Begins January 18, 2011
City Wilmington
Country USA

Event Recalls, Removals, and Market Corrections in Compliance with FDA and ISO Requirements - Webinar By GlobalCompliancePanel
Begins January 13, 2011
City Wilmington
Country USA

Event Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel
Begins January 13, 2011
City Wilmington
Country USA

Event 101 cGMP To-Do List for 2011 - Webinar By GlobalCompliancePanel
Begins January 12, 2011
City Wilmington
Country USA

Event FDA 483 Observations in the Laboratory. What went wrong? How can they be avoided? - Webinar By GlobalCompliancePanel
Begins January 12, 2011
City Wilmington
Country USA

Event The Process Approach to Auditing - Webinar By GlobalCompliancePanel
Begins January 11, 2011
City Wilmington
Country USA

Event A Comparison of ICH Q-10 Quality System and the FDAs Quality Systems Approach (QSA) to the Pharmaceutical GMPs - Webinar By GlobalCompliancePanel
Begins January 11, 2011
City Wilmington
Country USA

Event Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar By GlobalCompliancePanel
Begins January 11, 2011
City Wilmington
Country USA

Event Designing and Implementing a Dress Code - Webinar By TrainHR
Begins January 10, 2011
City Wilmington
Country USA

Event ISO 13485 as a Quality Management System for Medical Devices - Webinar By GlobalCompliancePanel
Begins December 16, 2010
City Wilmington
Country USA

Event The Advantages of Linking Management Systems - Webinar By GlobalCompliancePanel
Begins December 15, 2010
City Wilmington
Country USA

Event Audit Committee Responsibilities for Internal Controls - Webinar By GlobalCompliancePanel
Begins December 14, 2010
City Wilmington
Country USA

Event The 510(k) Submission: Requirements, Contents, and Options - Webinar By GlobalCompliancePanel
Begins December 8, 2010
City Wilmington
Country USA

Event The FDAs Working Group Reports, I & II - New Directions - Webinar By GlobalCompliancePanel
Begins December 8, 2010
City Wilmington
Country USA

Event Basics of OTC Drug Labeling Compliance - Webinar By GlobalCompliancePanel
Begins December 2, 2010
City Wilmington
Country USA

Event Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel
Begins December 2, 2010
City Wilmington
Country USA

Event Introduction to Operational Risk - Webinar By GlobalCompliancePanel.com
Begins December 1, 2010
City Wilmington
Country USA

Event Know Your Customer - The DEA Due Diligence - Webinar By GlobalCompliancePanel.com
Begins November 30, 2010
City Wilmington
Country USA

Event Understanding Acceptance Activities for Medical Devices - Webinar by GlobalCompliancePanel
Begins September 14, 2010
City Wilmington
Country USA

Event Physical Properties Analytical and Screening Techniques - Webinar by GlobalCompliancePanel
Begins September 14, 2010
City Wilmington
Country USA

Event Auditing API Manufacturers and Suppliers - Webinar by GlobalCompliancePanel
Begins September 14, 2010
City Wilmington
Country USA

Event Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel
Begins September 9, 2010
City Wilmington
Country USA

Event Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11 - Prepare Yourself - Webinar by GlobalCompliancePanel
Begins September 9, 2010
City Wilmington
Country USA

Event Key Modules of an Effective CAPA SOP - Webinar by GlobalCompliancePanel
Begins September 8, 2010
City Wilmington
Country USA

Event Effective & Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel
Begins September 8, 2010
City Wilmington
Country USA

Event Post-Design Medical Device Risk Management - Webinar by GlobalCompliancePanel
Begins September 7, 2010
City Wilmington
Country USA

Event Improving Sanitation Standard Operating Procedures in the Food Industry - Webinar by GlobalCompliancePanel
Begins September 7, 2010
City Wilmington
Country USA

Event Paranormal Investigation of the Battleship NC with GHI Cast Members
Begins August 20, 2010
City Wilmington
Country USA

Event April 29th – Out Impact’s New Professional Series, First Teleseminar Featuring NAGLREP
Begins April 29, 2010
City Wilmington
Country USA

Event GlobalCompliancepanel brings a new webinar on the topic of Business, Project and Compliance Risk
Begins March 2, 2010
City Wilmington
Country USA

Event Phantasm 2009
Begins September 10, 2009
City Wilmington
Country USA

Event 2009 Nursing Leadership Symposium
Begins June 5, 2009
City Wilmington
Country USA

Event HarrisMartins Delaware Asbestos Conference
Begins February 20, 2009
City Wilmington
Country USA

Event WiFi Film Conference
Begins June 27, 2008
City Wilmington
Country United States

Event Reaching New Heights: New Hanover Regional Medical Centers Inagural Nursing Leadership Symposium
Begins May 11, 2007
City Wilmington
Country USA

Event Third Annual Pain Management Symposium
Begins November 21, 2003
City Wilmington
Country USA

Event Fifth Annual Pediatric Conference - Focus on ADHD
Begins October 16, 2003
City Wilmington
Country USA

Event 11th Annual Coastal Oncology Symposium
Begins June 27, 2003
City Wilmington
Country USA

Event Risk-Based Validation for GxP Facilities - Webinar By GlobalCompliancePanel
Begins
City Wilmington
Country USA

Event Preventing Harassment in the Workplace - Webinar By TrainHR
Begins
City Wilmington
Country USA


 

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