The FDA Inspection: Preparation, Management, and Follow - up

Website https://www.compliance4all.com/control/w_product/~product_id=502276LIVE?channel=ourglocal_Mar_2019_S | Edit Freely

Category Product Development, Engineering, Manufacturing, Complaint Handling

Deadline: March 07, 2019 | Date: March 08, 2019

Venue/Country: Online, U.S.A

Updated: 2019-01-21 15:02:53 (GMT+9)

Call For Papers - CFP

This webinar is designed to teach participants how to utilized MBSR techniques as a means to reduce stress and burnout, promote positive workplace functioning, and improve job satisfaction and productivity.

Why should you Attend:

The FDA inspection is the most nerve-wracking event in the life of a regulatory professional - you're in charge of compliance, usually in the background, and NOW you're in the spotlight, and if your performance isn't good, it's not the show that may close, it's YOUR COMPANY!

Areas Covered in the Session:

Where do I let the inspector go?

Do I give them a tour?

What should I let them see?

Who should I let them talk to?

Are they ever going to leave?

Who Will Benefit:

Regulatory Compliance and Regulatory Affairs

Quality Management System

Quality Assurance

Quality Control

Product Development

Engineering

Manufacturing

Risk Management

Speaker Profile:

Jeff Kasoff , RAC, CMQ/OE is the Principal Consultant at Lean to Quality, LLC. He s has more than 30 years of experience in Quality and Regulatory management. Over that time, He has implemented and overseen quality system operations and assured compliance, at all sizes of company, from start-up to more than $100 million in revenue. This multi-faceted experience makes Jeff uniquely qualified to address compliance issues across the entire range of company sizes.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com