Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : Learn how to perform risk assessment as part of the risk-based approach to computer system validation.

Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This 3-hr virtual seminar on the Electronic Common Technical Document will help you understand the background, technical aspects, document structure, and use of the electronic Common Tech…

Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : Learn about HRQOL, the concept, strategies, process and how to interpret HRQOL results accurately.

Contact Person : admin; Last Date for the submission of abstract : Not Available ; Description : This ICF process Webinar training teaches how to create an informed consent process for achieving optimal site compliance and subject comprehension. It also discusses how an inadequate ICF can …

Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This 3-hr FDA Documentation training will focus on ideas that will help identify effective methods designed to improve your document control systems, for compliance in a regulated environ…

Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This webinar on Lyophilization Process Development and Cycle Design will cover the process and benefits of using an empirical approach to design an optimized lyophilization cycle.

Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This Japan Regulatory and Clinical Trial Requirements training will cover Japan Regulatory Agency Structure and Responsibilities, its review process for decision-making and approval, …

Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This 90-minute training on Major cGMP Issues for 2012 will show what drug and device companies can do proactively to address failures over cGMP issues and ensure better regulatory complia…

Contact Person : ComplianceOnline; Last Date for the submission of abstract : Not Available ; Description : This webinar on safety reporting in clinical trials will focus on the major revisions that FDA made to its IND safety reporting requirements.

Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This webinar on wage and hour law will focus on how to comply with Federal and State requirements as well as some local regulations that have been instituted recently.

Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This 6-hr virtual seminar will focus on the regulatory compliance requirements and procedures for conducting Clinical Trials on Pharmaceutical Products in South Korea. It will also cover …

Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : This EO sterilization training Webinar will discuss the important parameters to measure for the sterility assurance level and actions to take if they are not compliant to the process specifi…

Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : This EO sterilization training Webinar will discuss how to modify EO sterilization process for complicated medical products which are sensitive to moisture, temperature, vacuum changes.

Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : In this Device History Record (DHR) training learn how to avoid FDA 483?s Warning Letters and other compliance issues related to DHR compliance by knowing how risk management fits in to DHR …