Past Events (3,027)

Webinar On 21 CFR 11 Compliance for Excel Spreadsheets

October 21, 2014 from 1pm to 2:30pm – Online In Dec. 2010, the FDA has stepped up enforcement for 21 CFR 11 compliance with spreadsheets being considered as low hanging fruit for FDA inspectional findings. Spreadsheet Applications such as MS Ex… Organized by Compliance Trainings | Type: webinar

Webinar on Medical Devices Designing with Cleanliness in Mind

October 20, 2014 from 1pm to 2pm – Online event, Canada Cleanliness is a hot topic in the medical device industry. The FDA expects medical device companies to validate the cleanliness of their devices. One of the best ways to achieve a clean device is by… Organized by Compliance Trainings | Type: webinar

Webinar On Best Practices for 510(k) Drafting and Submission: Dos and Don'ts

October 17, 2014 from 1pm to 2pm – online event, Canada From this webinar you will learn best practices for adequately putting your 510(k) together for your successful submission to the FDA, compliant with the FDA’s eCopy and RTA policy. This session will… Organized by Compliance Trainings | Type: webinar

Webinar On FDA’s New Guidance On Medical Device Development Tools (MDDT)

October 9, 2014 from 1pm to 3pm – Online event, Canada This webinar will discuss a voluntary process for qualification of Medical Device Development Tools (MDDT) for use in device development. An MDDT is a scientifically validated tool (test) to determin… Organized by Compliance Trainings | Type: webinar

Live Webinar on FDA Adverse Event Reporting for Drugs and Medical Devices

September 25, 2014 from 1pm to 3pm – Online This web seminar presents an overview of FDA’s Adverse Event Reporting Systems for Drugs and Medical Devices. Adverse Event Reporting for Investigational Drugs/Medical Devices and post-approval Adver… Organized by compliancetrainings | Type: webinar
2-day In-person Seminar on “Effective Complaint Handling, Medical Device Reporting and Recalls and Avoiding Costly Errors” in Australia

September 25, 2014 at 9am to September 26, 2014 at 6pm – Hilton Sydney Hotel Detailed Description: An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be ev… Organized by John Robinson | Type: conference

Webinar on How to Implement HIPAA Requirements in GxP Regulated Establishments

September 17, 2014 from 1pm to 2:30pm – Online HIPAA, which stands for Health Insurance Portability & Accountability Act, does not just apply to health insurance. The rules apply to all companies with Personal Health Information (PHI) in elec… Organized by compliancetrainings | Type: webinar

Webinar On Risk Management Principles

September 15, 2014 from 1pm to 2pm – Online ICH Q9 Quality Risk Management issued in 2009 laid out the basic principles for risk management to be utilized in all areas of the pharmaceutical industry including clinical trials but also manufactu… Organized by compliancetrainings | Type: webinar
GMP Compliance for Pharmaceutical Quality Control Laboratories: 2-day In-person Seminar

September 15, 2014 at 9am to September 16, 2014 at 6pm – w hong kong Overview: This course is designed for people who are growing in their knowledge of pharmaceutical quality control practices and regulations. It will be a "how to" course where the instructor will exp… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda