Online Event worldwide

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Palo Alto, California 94301
August 14, 2009

Organization models for social media - Social Media Academy at Online Event worldwide

January 22, 2010

Social Media Methodology Round Table #2 - Career and Knowledge at Online Event worldwide

February 25, 2010

Paper Basics Workshop - 5 series (1 hour workshop per week) at Online Event worldwide

December 14, 2010

Vue2010 - Social media for Event Management at Online Event worldwide

January 19, 2011

Explore how the Social Media Academy can enhance your business & your career at Online Event worldwide

June 6, 2012

Unsolicited Drug and Device Off-Label Claims Via Social Media and Risk Management at Online Event worldwide

June 6, 2012

Verification and Validation (V&V) of Software in the Medical Devices at Online Event worldwide

June 8, 2012

3-hr Virtual Seminar: Legal Issues Impacting Human Resource Management at Online Event worldwide

June 13, 2012

Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations at Online Event worldwide

June 13, 2012

3-hr Virtual Seminar: The Psychology (and Law) of Harassment Investigations at Online Event worldwide

June 14, 2012

Common Concerns and Penalties Related to the Americans with Disability Amendments Act (ADAA) at Online Event worldwide

June 14, 2012

Auditing Systems for 21 CFR Part 11 Compliance: Preparing Yourself for Inspection at Online Event worldwide

June 14, 2012

REMS Update: Risk Evaluation and Mitigation Strategies at Online Event worldwide

June 15, 2012

The Investigational Medicinal Product Dossier (IMPD): EU's CTA vs. FDA's IND at Online Event worldwide

June 19, 2012

Complying with FLSA – How to Determine Exempt Status & Calculate Overtime Correctly at Online Event worldwide

June 19, 2012

The U.S. FDA's New Global Engagement Initiative - Webinar By ComplianceOnline at Online Event worldwide

June 19, 2012

Medical Device: Risk Assessment and Mitigation through FMEA at Online Event worldwide

June 20, 2012

An Introduction to Process Validation - For Beginners at Online Event worldwide

June 21, 2012

How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare at Online Event worldwide

June 22, 2012

Acceptance Sampling by Variables Using Z1.9 - Webinar By ComplianceOnline at Online Event worldwide

June 25, 2012

Ethics and Privilege Issues Under ERISA - Webinar By ComplianceOnline at Online Event worldwide

June 26, 2012

cGMPs for Medical Devices, Including In Vitro Diagnostic Devices at Online Event worldwide

June 28, 2012

Telecommuting: Effective Policies, Practices, and Programs at Online Event worldwide

June 28, 2012

FDA’s Regulation of Veterinary Regenerative Medicine at Online Event worldwide

June 28, 2012

Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems at Online Event worldwide

June 29, 2012

Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs at Online Event worldwide

June 29, 2012

3-hr Virtual Seminar: IND Applications for Phase I Studies at Online Event worldwide

July 2, 2012

Affirmative Action and Recent Trends within the OFCCP - Webinar By ComplianceOnline at Online Event worldwide

August 14, 2012

Biomarkers for Drug Development at Online Event worldwide

August 16, 2012

Updating Compliance for Design History Files of Older Products at Online Event worldwide

August 20, 2012

Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA at Online Event worldwide

August 21, 2012

Process Verification and Validation Planning and Execution at Online Event worldwide

August 21, 2012

Disinfectant Qualification and Cleanroom Disinfection at Online Event worldwide

August 22, 2012

Addressing Impurities in Pharmaceutical Products: Impurities, Degradants, Residual Solvents and Elemental Impurities at Online Event worldwide

August 22, 2012

The 6 Most Common Problems in FDA Software Validation & Verification at Online Event worldwide

August 23, 2012

Anticipated Changes to the EU Medical Device Directives; 2010 Changes and What the Future Holds for Licensees at Online Event worldwide

August 27, 2012

Site Challenges in Conducting Investigational Device Trials at Online Event worldwide

August 28, 2012

Laboratory Water Quality at Online Event worldwide

August 29, 2012

(QMS) Competence and Training Requirements per FDA QSR and ISO 13485 at Online Event worldwide

August 31, 2012

Reducing Ethylene Oxide (EO) Sterilization Costs While Maintaining Regulatory Compliance at Online Event worldwide

September 5, 2012

Validation and use of Excel spreadsheets in FDA regulated environments at Online Event worldwide

September 6, 2012

How to Investigate Environmental Monitoring Excursion Limits at Online Event worldwide

November 1, 2012

Non-inferiority Trials: Practical Issues and Current Regulatory Perspectives at Online Event worldwide

November 7, 2012

Risk Mitigation and Optimization Techniques for Drug Development Portfolio Planning at Online Event worldwide

November 9, 2012

Data Monitoring: Meeting the Needs and Requirements of Sponsors and IRBs at Online Event worldwide

November 9, 2012

South Korea - Navigating the South Korean Regulatory Compliance and Clinical Trial Environment at Online Event worldwide

February 15, 2013

The Psychology and Law of Workplace Misconduct: From the Manipulative to the mentally ill at Online Event worldwide

May 2, 2013

The 510(k) Submission: Requirements, Contents, and Options at Online Event worldwide