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This question was asked for Webinar - Understanding Disinfectant Qualification Studies - How To Avoid Errors
05-28-2013 11:05am by: Justin jolly

  0 0 Biotechnology
OTC monograph annual report
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
ANDA OTC, prescription RLD NDA approved products
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
Monographed product changes reporting
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
OTC monographed product registration process
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
OTC drug registration-U.S. agent requirements and responsibilities
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
Post approval change requirements of monographed products
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
Conveying regulatory status of products grandfathered into the monograph
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
Post approval changes to non-monograph OTCs
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
New ingredient or labeling statement addition to an existing monograph
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
FDA requirements for NDAs and monographs
05-17-2013 04:05am by: Co attendee

May 17, 2013
by: Coexpert
1 1 Drugs and Chemicals
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