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?

Date : 17th October 2017 to 17th October 2017

Place : United States, Fremont

Website :http://www.compliance4all.com/control/w_product/~product_id=501416LIVE?channel=allconferencealerts_Oct_2017_SEO

Contact Person:Event Manager

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?

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? will be held in Fremont,United States on date 2017-10-17

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Deadline for abstracts/proposals : 16th October 2017

Keynote Speakers :

Venue :Fremont, CA, United States

Check the event website for more details.