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Title, Username & Date Rating  Last Post  Replies 
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Basis for testing 10 lots; Raw Material; GMP Guidelines
05-01-2013 01:05am by: Co attendee

May 01, 2013
by: Coexpert
1 1 All FDA Regulated Industry
Changing Solvents; Raw Material Testing; GMP Guidelines
05-01-2013 01:05am by: Co attendee

May 01, 2013
by: Coexpert
1 1 All FDA Regulated Industry
Raw material change report submission to the FDA
05-01-2013 01:05am by: Co attendee

May 01, 2013
by: Coexpert
1 1 All FDA Regulated Industry
Raw material GMP certification from the vendor
05-01-2013 01:05am by: Co attendee

May 01, 2013
by: Coexpert
1 1 All FDA Regulated Industry
Raw material- international vendor
05-01-2013 01:05am by: Co attendee

May 01, 2013
by: Coexpert
1 1 All FDA Regulated Industry
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
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