Mon, Nov 07
|Toronto
Validation & GMP University Canada
Join Compliance Associates for Validation & GMP University series tailored specifically for those manufacturing drugs, biologics, and medical devices in Canada. The event provides hands-on training for Quality, Validation, Engineering and Regulatory Affairs professionals.
![Validation & GMP University Canada](https://static.wixstatic.com/media/b07308_7268f57b53b34b6aac5d385fc198f90e~mv2.png/v1/fill/w_980,h_512,al_c,q_90,usm_0.66_1.00_0.01,enc_auto/b07308_7268f57b53b34b6aac5d385fc198f90e~mv2.png)
![Validation & GMP University Canada](https://static.wixstatic.com/media/b07308_7268f57b53b34b6aac5d385fc198f90e~mv2.png/v1/fill/w_980,h_512,al_c,q_90,usm_0.66_1.00_0.01,enc_auto/b07308_7268f57b53b34b6aac5d385fc198f90e~mv2.png)
Time & Location
Nov 07, 2022, 8:00 a.m. EST – Nov 08, 2022, 7:00 p.m. EST
Toronto, 37 King St E, Toronto, ON M5C 1E9, Canada
About the event
Participants create-their-own-experience by choosing from over 30 tutorials offering innovative, modern strategies for Validation and Quality Systems Management. Whether you’re interested in best practices for process, cleaning, and computer validations, or quality metrics, change control and risk management, this conference is for you! Come join the fun and learn from the best SMEs our industry has to offer and enrich your professional development in these critical environments.
- Navigate the maze of validation regulatory guidance – A systematic approach to knowledge management
- Design a risk-based IQ, OQ, and PQ approach for facility commissioning & equipment qualification
- Modernize software validation – Align with CSA, risk assessments, and critical thinking
- Change Control – Mitigate risk when making changes to validated systems
- Continued Process Verification – Maintaining equipment and processes in a validated state
- Analytical testing for process validation
- Risk-based process validation – Program implementation case study
- QRM – Conducting a validation risk assessment
- Qualify critical utility systems – HVAC, Water and Gas
- Medical device validation & verification program implementation
- Build a Data Integrity program from the ground up
- Developing a high-quality Validation Master Plan (VMP) for regulators
- Risk-based supplier partnering and auditing – During the Pandemic and Beyond