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Expectations of Regulatory & Validation Master Planning - 2017

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Website http://www.compliance4all.com/control/w_product/~product_id=501357LIVE?channel=ourglocal_Jul_2017_SE | Edit Freely

Category Validation Master Planning, Quality System Documentation, Pharmaceutical Industries, Quality Assurance, Quality Control, Validation, validation master plan software, Regulatory expectations

Deadline: July 19, 2017 | Date: July 20, 2017

Venue/Country: Online, U.S.A

Updated: 2017-05-16 20:29:45 (GMT+9)

Call For Papers - CFP

Overview:

This presentation will cover the importance of master planning. The FDA and other regulatory bodies expect these to be among the Quality System documentation.

Areas Covered in the Session:

History and background

Types

Organization

Requirements

Regulatory expectations

Maintenance

Who Will Benefit:

Compliance Personnel

QA Personnel

validation Personnel

Speaker Profile:

Louis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of experience in Quality Assurance, Quality Control, Validation, consent decree remediation as well as cGMP Compliance in the Medical Device and Pharmaceutical industries.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.