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| iRegulatory is a pharmaceutical regulatory affairs consultancy with extensive
publishing experience. We have submitted many dossiers in paper, eCTD and
other electronic formats through the Centralised (CP), Decentralised (DP)
and Mutual Recognition Procedures (MRP), as well as Responses to Questions,
amendments/variations and Clinical Trial Applications (CTA’s). These submissions
have covered many indications and include novel, generic, bio-similar and
veterinary products.
2008-7-1 00:00:00 GMT+00:00Countdown to 'electronic-only' submissions for the EMEA, see below for further information.
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