1. Live Webinar on : Document Approval, Control, and Distribution:How to Develop a
Compliant, Cost Effective System Tuesday,March 06, 2012
duration : 01:00 to 02:00 PM EST
Get 15 % Discount as a early bird
registrations. Use Promo Key :
CGO15
Who will benefit
Executive Management
Document Control Management
Document Control Clerks
Consultants
Quality system auditors
purchase formats
$189 One Dial In - One
Attendee
Description
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

2. $249 One Dial In - Unlimited
attendance (To be arranged in a
Conference room/Meeting room.
Note : Only One Dial In Allowed)
$289 On Demand (Recording
available within 48 hrs after the
completion of the webinar)
$349 Get Training CD
More Trainings
- Immediate document distribution
Who will benefit:
This webinar will providevaluable assistanceto all regulated
companies that are interested in learningaboutthe
requirements for a document control system, and spending
less time on its implementation and performance. The
employees who will benefitinclude:
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.
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