Change Control Systems for Medical Devices Current Best Practices for FDA-Compliant Systems - Compli (Medical Device)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Jan 18, 2011 End Date/Time: Jan 18, 2011
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Why You Should Attend:

It is well known that document change control is a critical requirement for FDA-regulated companies. However, this can be a time- and paper-consuming process, in which even the simplest of changes requires an inordinate amount of time spent in the preparation, submission, distribution, and implementation of change requests, document modifications, document review meetings, document approvals, and document placement. The best document change control systems are those that are fast and effective.

This presentation will review the QSR requirements for document change control, and provide a streamlined process - Many companies can spend MUCH LESS preparing MANY FEWER documents, and still be in compliance with the regulations; is yours one of these?

Areas Covered in the Seminar:

QSR requirements for document change control.
Description of typical document change control system in use.
Streamlined document change control process.
Paper-free document review.
Immediate document distribution.
Paper-free document management system.
Document change requests: submission, processing, and review.
Document change approval and distribution.
How to handle "Minor" changes.
Streamlined document change control process.
Change control for design documentation.

Note: Use these promocode(117660) for 10% discount.


Online Event
2600 E. Bayshore Road
Palo Alto
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