Live webcast on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)

FOR IMMEDIATE RELEASE
Houston, Texas, United States of America (Free-Press-Release.com) January 19, 2012 -- Document Approval, Control, and Distribution: How to Develop a Compliant, Cost Effective System
Description
Discount: Get 15 % Discount as a early bird registrations. Use Promo code CGO15
Tuesday, March 06, 2012

It is well known that document control is a critical requirement for FDA-regulated companies. However, document control 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 control systems are those that are fast and effective. This presentation will review the QSR and ISO requirements for document 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 Session:

- QSR and ISO 13485 requirements for document control

- Description of typical document control system in use

- Streamlined document control process

- Paper-free document review

- Immediate document distribution

Who will benefit:

This webinar will provide valuable assistance to all regulated companies that are interested in learning about the requirements for a document control system, and spending less time on its implementation and performance. The employees who will benefit include:

Executive Management
Document Control Management
Document Control Clerks
Consultants
Quality system auditors



About Speaker

Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy products. In this position, Jeff is responsible for supplier management, during which he oversees supplier management, CAPA, and document control. Prior to this, Jeff spent 13 years at Life-Tech as the Director of Regulatory Affairs, where he was responsible for regulatory compliance of all aspects of the quality system. Jeff received his regulatory affairs certification in 1996.


Purchase formats: Live: $189.00 One Dial In - Unlimited attendance $249 Recorded: $289.00, CD: $349.00
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https://compliance2go.com/index.php?option=com_training&speakerkey=15&productKey=34