All Events in Canada (25)

Webinar On - How to select Software for a Regulated Environment

March 24, 2014 from 12pm to 1pm – Canada Description: Software is widely used in our industry and selection of new software or upgrade of existing software is one of the activities that crop up every year in an IT department’s task list. Ou… Organized by compliancetrainings | Type: online, webinar

Webinar On FDA proposed changes to ISO 13485: 2015 and Medical Devices Quality Management Systems

December 9, 2014 from 1pm to 2:30pm – Canada Description : ISO 13485:2015 - What’s coming? Understand proposed changes being worked on by the ISO technical committee for updating the ISO 13485:2003. Awareness of the current requirements and pro… Organized by Compliance Trainings | Type: webinar

Webinar On Statistical Process Control (SPC)

January 20, 2015 from 1pm to 2pm – Canada Description : All companies want to improve the quality of their products. Attempts to improve product quality need to be structured in such a way that they have a reasonable chance of success and th… Organized by Compliance Trainings | Type: webinar

Webinar On Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs

April 16, 2015 from 1pm to 2pm – Canada Description : The US Food and Drug Administration (FDA) states in warning letters “this inspection revealed that these devices are adulterated within the meaning of section 510(h) of the FD&C Act… Organized by Compliance Trainings | Type: webinar

Webinar On Cleaning Validations Using Extraction Techniques

April 20, 2015 from 1pm to 2pm – Canada Description : Medical device manufacturers have always been under scrutiny to ensure that their product does no harm to the patient. Regulatory agencies have become increasingly aware of the potenti… Organized by Compliance Trainings | Type: webinar

Webinar On A Robust Approach to Validation in Compliance with 21 CFR, Part 820.75

April 23, 2015 from 1pm to 2pm – Canada Description : Regardless or regulatory environment, United States or OUS, the validation of processes, which cannot be verified through inspection or test, is considered a salient requirement for med… Organized by Compliance Trainings | Type: webinar

Webinar On Drug Development & Discovery by FDA Standards

April 27, 2015 from 1pm to 2pm – Canada Description : The Drug Discovery and Development (but also the biologics and medical device) process is a very complex process with every participant focusing on their particular piece of discovery o… Organized by compliancetrainings | Type: webinar

Webinar On Managing Product and Process Risk through Failure Mode and Effects Analysis (FMEA)

April 29, 2015 from 1pm to 2pm – Canada Description : Conducted early in the process development cycle, the Failure Modes and Effects Analysis tool is used to identify risks and then adjust the manufacturing or service process to reduce th… Organized by Compliance Trainings | Type: webinar
Webinar On Method Validation: Utilizing Quality by Design (QbD) and Risk in Implementation

April 29, 2015 from 1pm to 2pm – Canada Description : Pharmaceutical industry is experiencing a growing need to improve performance driven by global competition and the increasing impact of information technology. FDA’s Process Validation… Organized by Compliance Trainings | Type: webinar

Webinar On Upcoming HIPAA Audits - How to avoid and be prepared

May 5, 2015 from 1pm to 2pm – Canada Description : HIPAA NOW HAS TEETH ! Be prepared ! Protect your practice or business ! What factors might spurn a HIPAA audit? …are you doing these things? Why are the Feds enforcing after all these y… Organized by Compliance Trainings | Type: webinar