Validation Program to a Building from Top to Bottom - 2017

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Category Software Validation Process, 2017 Webinars, Auditing, compliance trainings, 2017 software online courses, quality validation programs, Engineering Department trainings, Validation Engineers and Managers, FDA checklist 2017

Deadline: August 03, 2017 | Date: August 04, 2017

Venue/Country: Online, U.S.A

Updated: 2017-06-15 15:11:20 (GMT+9)

Call For Papers - CFP

Many more typical questions are now available in this simple to understand,

yet detailed training session designed to help manufacturers of FDA

regulated products build a sustainable validation program.

Why you should attend:

How PLC-based systems or laboratory equipment should fall within the

methods validation program, software validation program, or even the

equipment qualification program.

Areas Covered In the Session:

Discuss what FDA is really looking for in process validation

Specify the deliverables associated with software validation

Common pitfalls to avoid when executing validation protocols

How to estimate costs and time associated with validation

Who will benefit:

Internal Auditors

Senior Management

Compliance Officers

QA Managers

QC Managers

Purchasing Managers

Speaker Profile:

Jonathan M. Lewis has over twenty-two years’ experience in the areas of

executive management, quality control (QC), quality assurance (QA),

manufacturing, regulatory affairs, validation, and project management in

both industry and consulting roles. Mr. Lewis has experience in the medical

device, diagnostic, biopharmaceutical, pharmaceutical, cosmetic, dietary

supplement, food, and animal food industries.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com