 |
 |
 |
 |
 |
 |
 |
 |
|
|
 |
|
|
What You Will Learn:
Gain a broad picture of the medical device standard and how it is being implemented. Become familiar with other related standards such as Risk Management. Find out the global trend in medical devices standards.
Who Should Attend:
Managers and Directors in charge of assessing whether their organization should embark on the ISO 13485 Medical Standard for their organization. Also, people who wish to develop a plan to implement this standard.
Duration:
One day Seminar, also available on-site
CEU: 0.8 units
Check out our training schedule for seminars.
About the Seminars (Hours, Fee Structure, Location, How to register)
Seminar Outline:
- Interpreting all clauses of ISO 13485:2003
- Comparing ISO 13485 to ISO 9001:2000
- Introduction to Risk Management and ISO 14971
- Introduction to Medical Device Regulations in Canada, US and the European Union
Please call or e-mail today at (416) 667-9119 or info@grt77.com for information and further details.
G.R. Technologies
1110 Finch Ave. West, Suite 516
Toronto, Ontario
M3J 2T2
E-mail: info@grt77.com
Tel: (416) 667-9119
Fax: (416) 667-1288