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Complete Response Letters (CRLs): Big Trouble For Small Pharma

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A recent EP Vantage analysis of publicly-reported Complete Response Letters (CRLs) issued by the FDA from 1 January 2017 until 30 May 2018 had surprising results. The analysis found that small companies received most of the CRLs issued during this period

....So why are smaller small/specialty pharma companies struggling to get first cycle 505(b)(2) approvals? Several factors may be involved in the overrepresentation of small pharma in the CRL list.

Regulatory expertise: EP Vantage suggests smaller companies struggle to recruit staff with appropriate regulatory expertise.
Lack of Familiarity: A perception that approval of a new indication or dosage form of an approved drug will be straightforward. This can be an overly optimistic judgement without appropriate and extensive 505(b)(2) regulatory expertise. Problems can arise with CMC, bridging, and justifying public data that are not encountered in traditional 505(b)(1) programs.

om een beetje kennis op te doen,

camargopharma.com/2018/06/complete-re...

...."suggests smaller companies struggle to recruit staff with appropriate regulatory expertise" zou het daar aan gelegen hebben bij Pharming en denkende dat het Product al op de markt was.
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