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FDA and ISO Compliance Personnel Training - 2017

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Category FDA and ISO Compliance, Employee Training, Regulatory Webinars, quality system operations, Quality and Regulatory management, regulatory management software courses, Compliance trainings, regulatory affairs management

Deadline: July 16, 2017 | Date: July 17, 2017

Venue/Country: Online, U.S.A

Updated: 2017-05-16 20:28:00 (GMT+9)

Call For Papers - CFP


To satisfy QSR and ISO 13485 requirements as well as produce quality products, companies must assure personnel are trained on their routine job practices as well as familiar with requirements that impact them.

Areas Covered in the Session:

Regulatory requirements for personnel training

Establishment of a training program

New employee training

Methods of training

Who Will Benefit:

Personnel who perform training

Personnel who receive training

Low-mid level management

Regulatory Affairs personnel

Human resources (HR) staff

Speaker Profile:

Jeff Kasoff, RAC, CMQ/OE has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operations and assured compliance, at all sizes of company, from startup to more than $100 million in revenue.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407


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.