Date: | October 17, 2017 - 10:00am - 11:00am |
Timezone: | (GMT-08:00) Pacific Time (US & Canada) |
Location: | Fremont, CA, 94539, United States, 161 Mission Falls Lane, Suite 216 |
Website for Event: | http://www.compliance4all.com/control/w_product/~product_id=501416LIVE?channel=s... |
Topic: | Health Education |
Description: | Overview:In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Why should you Attend:The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for analytical equipment qualification and validation in your facility? Areas Covered in the Session: Who Will Benefit: Speaker Profile:Joy McElroy Upon earning a degree in Zoology at North Carolina State University, Joy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their uality Control Lab. Contact Detail: |
Contact Name: | Event Manager |
Contact Email: | support@compliance4All.com |
Contact Phone: | 8004479407 |