Best Practices & Effective Cleaning Validation Procedures - 2017

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Category Pharmaceutical, Validation Programs, Quality Auditing Programs, checklist of gmp compliance auditing, gmp compliance audit, pharmaceutical industry, Quality professionals, regulatory inspections, Compliance trainings

Deadline: September 13, 2017 | Date: September 14, 2017

Venue/Country: Fremont, U.S.A

Updated: 2017-07-17 16:00:31 (GMT+9)

Call For Papers - CFP

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 Cleaning Validations of your manufacturing equipment?

Areas Covered in the Session:

Understand the FDA perspectives on cleaning validation and areas of concern during regulatory inspections

Be able to set up cleaning validation procedures, protocols and reports that meet current FDA, WHO, PIC/S and EU regulations

Prepare and defend your own cleaning validation approach/program and avoid costly delays and/or rejections by regulatory agencies

Who Will Benefit:

Senior Quality Managers

Quality Professionals

Production Supervisors

Validation Engineers

Process Owners

Quality Engineers

Quality Auditors

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 Quality Control Lab.

Event Cost & Details:

One Dial-in One Attendee Price: US$150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com