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ectdexperts 06.02.2012, 19:42
New draft version of technical EU eCTD/NeeS validation criteria released for consultation http://t.co/mbaXH04Y
ectdexperts 06.02.2012, 14:37
#FDA updates eSubmitter Quick Guide and User Manual http://t.co/OaW3j79o
ectdexperts 03.02.2012, 12:15
thanks @shakulbio, @kathie_clark, @eSubmissions for the mentions
ectdexperts 01.02.2012, 18:48
EMA informs stakeholders about reduced data requirements for XEVMPD http://t.co/VNCpij5u #EVMPD
ectdexperts 01.02.2012, 16:17
#CDISC Standards in the Regulatory Submission Process http://t.co/TymrNRAt
ectdexperts 01.02.2012, 14:50
CDER Small Business Electronic Documentation Webinar, January 23, 2012 http://t.co/4Btu21aO
ectdexperts 01.02.2012, 14:47
@fxtrans: Meeting the linguistic requirements for EMA submissions http://t.co/Bmczs37o
ectdexperts 31.01.2012, 20:05
EVMPD to face reduced requirements: SSI optional, attachments SPC only - "common" EN sufficient for MRP/DCP. More soon
ectdexperts 26.01.2012, 22:10
26.01.2012 UK drug regulator MHRA details their technical validation process for #eCTDs http://t.co/xnJX4Til
ectdexperts 25.01.2012, 22:30
@kathie_clark: FDA re-issues PDF Spec V3.1 to clarifiy language on acceptable PDF versions for documents, add page numbers #ectd htt ...

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