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Title, Username & Date Rating  Last Post  Replies 
Expert
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Category
Raw material sampling from single lot
05-01-2013 12:05am by: Co attendee

May 01, 2013
by: Coexpert
1 1 All FDA Regulated Industry
CAPA report- Accepting probable cause
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
Recommended format for SCAR
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
Risk assessment document updation inclusion in closed-loop CAPA system
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
Differences between CAPA and routine investigation
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
Root causes identification and probable cause, FDA acceptance of probable cause
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
Using teams for CAPA investigations
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
CAPA audits- FDA 483s, corporate management responsibility
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
CAPA information application on GLP and GMP
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
CAPA audits compliance issues
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
Root Cause Analysis Tools- Flow chart, Ishikawa diagram, histogram, rectangle, oval, circles
04-30-2013 11:04pm by: Co attendee

Apr 30, 2013
by: Coexpert
1 1 Medical Devices
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