Analytical Instrument Qualification and Validation Processes - 2017

7 years ago Posted By : User Ref No: WURUR14100 0
  • Image
  • TypeWebinar
  • Image
  • Location Fremont, California, United States
  • Price
  • Date 17-10-2017
Analytical Instrument Qualification and Validation Processes - 2017, Fremont, California, United States
Webinar Title
Analytical Instrument Qualification and Validation Processes - 2017
Event Type
Webinar
Webinar Date
17-10-2017
Location
Fremont, California, United States
Organization Name / Organize By
Netzealous LLC DBA - Compliance4All
Organizing/Related Departments
Healthcare Training
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Finance

Information Technology

Accounting/Financial/Banking/Insurance

Medical/Healthcare/Hospital

Location
Fremont, California, United States

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:

  • Risk based Validation Approach
  • Going Through the Qualification Phases
  • User Requirements, Writing the Specifications
  • Testing and Deviation Handling
  • Proper Documentation

Who Will Benefit:

  • Quality Professionals
  • Regulatory Professionals
  • Compliance Professionals
  • Production Supervisors
  • Validation Engineers
  • Manufacturing Engineers
  • Production Engineers

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:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

Others Details

For more details and updates please visit website.

Registration Fees
Available
Registration Fees Details
One Dial-in One Attendee Price: US$150.00
Registration Ways
Email
Phone
Website
Address/Venue
  Online 
Official Email ID
Contact
Event Manager

Online

[email protected]

     18004479407
   Fax No: 302-288-6884