Date: | January 29, 2019 - 9:00am - 12:00pm |
Timezone: | (GMT-08:00) Pacific Time (US & Canada) |
Location: | 161 Mission Falls Lane, Suite 216,, Fremont, CA, 94539, United States |
Website for Event: | https://www.compliance4all.com/control/w_product/~product_id=502268LIVE?channel=... |
Topic: | Learning |
Description: | Overview: Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements. Why should you Attend: providing the product safety or efficacy seemingly promised. For most companies, the fixes are not rocket-science, but proper up-front V&V planning and execution, documented in a corporate MVP and implemented by other V&V documents. Areas Covered in the Session: Who Will Benefit: Speaker Profile: has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. Event Fee: One Dial-in One Attendee Price: US $290.00 Contact Detail: |
Contact Name: | Event Manager |
Contact Email: | compliance4all14@gmail.com |
Contact Phone: | 8004479407 |