Online Events

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June 7, 2012

Live webinar on SOP and FDA Compliance by compliance2go at Online Events

June 12, 2012

Live webinar on An Approach to Fair Lending and UDAAP By Compliance2go at Online Events

June 13, 2012

Live webcast on 21 CFR Part 11: Audit Trails – Ins and Outs By Compliance2go at Online Events

June 14, 2012

Live webinar on Import Compliance- How to Reduce Your Import Risks By Compliance2go at Online Events

June 18, 2012

Live webinar on Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By Compliance2go at Online Events

June 19, 2012

Live webinar on New Rules for HIPAA Business Associates: How the changes to HIPAA create new compliance obligations By compliance2go at Online Events

June 20, 2012

Live webinar on How to Manage a Medical Device Recall Efficiently and Effectively By Compliance2go at Online Events

June 21, 2012

Live webinar on Managing the Medical Device Supply Chain By compliance2go at Online Events

June 26, 2012

Live webinar on Best Practices in Document Control By compliance2go at Online Events

June 28, 2012

Live webinar on Effective Root Cause Analysis and CAPA Program by compliance2go at Online Events

July 3, 2012

Live webinar on nBest Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals By Compliance2go at Online Events

July 10, 2012

Live webinar on 21 CFR Part 11 Add-On Inspections by the FDA BY Compliance2go at Online Events

July 12, 2012

Live webinar on Update On and Look Ahead At FDA’s Changes to the 510(k) Process By Compliance2go at Online Events

July 19, 2012

Live webinar on Medical Device Adverse Event Reporting in EU, Canada and US By compliance2go at Online Events

July 24, 2012

Live webinar on FDA Regulation of Mobile Medical Apps By Compliance2go at Online Events

July 25, 2012

Live webinar on Best Practices for Complaint Handling in Compliance with FDA and ISO Regulations By Compliance2go at Online Events

July 26, 2012

Live webinar on Effective SOP Writing To Be FDA Compliant By Compliance2go at Online Events

July 31, 2012

Live webinar on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) By Compliance2go at Online Events

August 2, 2012

Live webinar on FDA Compliant Good Laboratory Practice (GLP) For Drugs, Biologics, Biosimilars and Medical Devices By Compliance2go at Online Events

August 2, 2012

Live webinar on Excel Spreadsheet Compliance with 21 CFR 11 By Compliance2go at Online Events

August 9, 2012

Live webinar on Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained By Compliance2go at Online Events

August 16, 2012

Live webinar on US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus By Compliance2go at Online Events

August 21, 2012

webinar by Compliance2go on China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations at Online Events

August 23, 2012

Webinar on Harmonized Tariff Schedule Classification By Compliance2go at Online Events