FDA inspectional - Training Practices for FDA Compliance - 2017

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Category FDA Compliance, Regulatory Trainings, FDA Webinars, Effective Training Practices, Regulatory affairs, Validation specialists, requirements in US and EU, training program, Compliance Trainings, Online Trainings, usa fremont compliance4all webinar 2017

Deadline: September 20, 2017 | Date: September 21, 2017

Venue/Country: Fremont, U.S.A

Updated: 2017-07-17 16:03:11 (GMT+9)

Call For Papers - CFP

Trainings are either not planned, not conducted, not evaluated or not documented as expected by inspectors. On the other hand it has been is estimated that about 5% of employee's time is spent for training.

Areas Covered in the Session:

GxP training requirements in US and EU

Most frequently cited deviations

Developing an effective training program for a company, site or department

Developing a training plan for individual employees

Who can or should be responsible for the training program and training plans

Who Will Benefit:

Training Departments

QA Managers and Personnel

Analysts and Lab Managers

Validation Specialists

Regulatory Affairs

Speaker Profile:

Ludwig Huber Ph.D., is the director and editor of Labcompliance the global online resource for validation and compliance. He is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems, Informa Healthcare".

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