Licensing failure in the European decentralised procedure

Publication date

2016-05-25

Authors

Langedijk, J.ISNI 000000049322810X
Ebbers, H.C.ISNI 0000000388591660
Mantel - Teeuwisse, AukjeISNI 0000000390595150
Kruger-Peters, Alexandra G
Leufkens, H.G.ISNI 0000000392454327

Editors

Advisors

Supervisors

Document Type

Article
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License

taverne

Abstract

The majority of the licensing applications in the European Union are submitted via the decentralised procedure. Little is known about licensing failure (i.e. refusal or withdrawal of a marketing authorisation application) in the EU decentralised procedure compared to the EU centralised procedure and the approval procedure in the United States. The study aim was to determine the frequency of and determinants for licensing failure of marketing authorisation applications submitted via this procedure. We assessed procedures that failed between 2008 and 2012 with The Netherlands as leading authority and assessed the remaining major objections. In total 492 procedures were completed, of which 48 (9.8%) failed: 8 refused, 40 withdrawn. A wide variety of major objections was identified and included both quality (48 major objections) and clinical (45 major objections) issues. The low failure rate may be related to the regular interaction between competent authorities and applicants during the procedure. Some degree of licensing failure may be inevitable, as it may also be affected by the financial feasibility or willingness to resolve major objections, as well as other reasons to withdraw an application besides the raised major objections.

Keywords

Marketing authorization, Failure, Generic, Bioequivalence, Therapeutic equivalence, Decentralized procedure, Taverne

Citation

Langedijk, J, Ebbers, H C, Mantel-Teeuwisse, A K, Kruger-Peters, A G & Leufkens, H G M 2016, 'Licensing failure in the European decentralised procedure', European Journal of Pharmaceutical Sciences, vol. 87, pp. 47–51. https://doi.org/10.1016/j.ejps.2015.10.014