FDA 2011 - Effective Documentation for Compliance in a Regulated Environment

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Category FDA Documentation; FDA Compliant Documentation; Documentation Guidelines; Documentation procedure; FDA guidelines; Documentation Standards; document control systems

Deadline: December 08, 2011 | Date: December 08, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2011-11-15 20:54:40 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

Since regulatory inspectors look very closely at critical documentation, it is imperative to develop a standardized and systematic system that ensures proper control and accuracy of your reports, procedures, and other important documents.

Do your reports completely explain the relevant issues?

Are your SOPs accurate, relevant, and useful to your operators?

Do your employees maintain proper control over your documents?

Areas Covered in the Seminar:

- Understand the basis for complete documentation.

- Review the most likely areas for scrutiny.

- Establish effective systems that will pass inspections with ease.

- Define adequate control measures to ensure compliance.

- Determine proper review techniques for records and reports.

- Rehearse effectively for regulatory audits.

NOTE : Use this Promocode (128600) to avail 10% discount, valid upto 6th December 2011.