eCTD Submissions for ANDAs, 505(b)(2)s, DMFs and ASMFs
14–15 May 2013
This intensive workshop is specifically tailored to the needs of companies preparing Abbreviated New Drug Applications (ANDAs), 505(b)(2)s, and Drug Master Files (DMFs) in eCTD format for the US Food and Drug Administration (FDA).
Discounted Registration Deadline: 12 April 2013
Advance Registration Deadline: 7 May 2013
On-site Registration Available: No
Please note that capacity for this program is limited. RAPS encourages participants to register early to confirm participation.
Cancellation Deadline: 12 April 2013
Questions? Call RAPS Solutions Center at +1 301 770 2920, ext. 200, or email firstname.lastname@example.org.