Compliance Online events

Compliance Online is focused on enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality and safety. Here are their latest listings:

29 Mar 2012Foreign Manufacturing Facilities - Avoiding Problems with FDA (Added 23 Feb 2012)
10 Apr 2012Issue Detection and Escalation in Clinical Trial Settings (Added 21 Feb 2012)
05 Jun 2012ICH Q10; moving from GMPs to a Pharmaceutical Quality System (Added 16 Feb 2012)
15 Apr 2012Full-day Virtual Seminar: How to Establish A Medical Device Quality System (Added 15 Feb 2012)
21 Mar 2012Best Practices for Maintaining an IND and IDE Application with FDA (Added 14 Feb 2012)
09 Mar 2012FDA's Rules for Financial Disclosure in Clinical Trials Clarified: New Guidance, Practical Application (Added 14 Feb 2012)
04 Apr 2012You have a Sterility Failure or Bioburden Excursion - Now What? (Added 06 Feb 2012)
07 Mar 2012When Do You Need a 510K? (Added 06 Feb 2012)
01 Mar 2012Basics of Testing Associated with Sterilization Validation and Routine Processing (Added 06 Feb 2012)
07 Mar 2012Method Validation in Drug Development Process - Common Mistakes and Issues (Added 03 Feb 2012)
20 Mar 2012How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices (Added 03 Feb 2012)
06 Mar 2012Audit/Inspection Preparedness for Clinical Research/Site Coordinators (Added 03 Feb 2012)
06 Mar 20123-hr Virtual Seminar: Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada (Added 02 Feb 2012)
29 Feb 2012Solutions to the Challenges of Phase I and FIM Studies in Today's World (Added 02 Feb 2012)
28 Feb 2012Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials (Added 02 Feb 2012)
22 Feb 2012Implementation of Pharmacogenomics into the Routine Clinical Laboratory (Added 27 Jan 2012)
28 Feb 2012Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results (Added 24 Jan 2012)
15 Feb 2012CRO or ARO: How to Hire and Manage One (Added 20 Jan 2012)
23 Mar 2012Elegant Quality Assurance Practices for Device Efficacy and Efficiency Requirements (Added 13 Jan 2012)
20 Mar 2012Project Management To Meet CGMP Requirements (Added 13 Jan 2012)
23 Feb 2012Understanding Design Controls for Medical Devices (Added 13 Jan 2012)
20 Feb 2012Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction (Added 13 Jan 2012)
16 Feb 2012Complaint Handling in Compliance with FDA and ISO Regulations (Added 13 Jan 2012)
07 Feb 20123-hr Virtual Seminar: Medical Device Regulations and Law in the US, EU and Canada (Added 13 Jan 2012)
13 Feb 2012Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations (Added 13 Jan 2012)
02 Feb 2012Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems (Added 13 Jan 2012)
27 Jan 2012Full-day Virtual Seminar: Analytical Procedures and Procedures Transfer (Added 13 Jan 2012)
20 Jan 20123-hr Virtual Seminar: An Introduction to the FDA New Drug Approval Process (Added 13 Jan 2012)
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