2006
DOI: 10.1016/j.indmarman.2005.06.001
|View full text |Cite
|
Sign up to set email alerts
|

New product development process and time-to-market in the generic pharmaceutical industry

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

0
29
0

Year Published

2009
2009
2022
2022

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 57 publications
(29 citation statements)
references
References 34 publications
0
29
0
Order By: Relevance
“…This phase starts with an experimental and accelerated stability study, with development based on a laboratorial scale including the (pilot) bio-equivalent-study and development of primary packaging. A scale-up from the laboratorial to the semi-industrial scale is performed (Cross, 2008;Prašnikar and Škerlj, 2006;Wheelwright, 2010;Witell et al, 2014). However, as shown in Figure 1, this research discovered that this phase itself consists of three parallel paths.…”
Section: The Npd Processmentioning
confidence: 97%
See 2 more Smart Citations
“…This phase starts with an experimental and accelerated stability study, with development based on a laboratorial scale including the (pilot) bio-equivalent-study and development of primary packaging. A scale-up from the laboratorial to the semi-industrial scale is performed (Cross, 2008;Prašnikar and Škerlj, 2006;Wheelwright, 2010;Witell et al, 2014). However, as shown in Figure 1, this research discovered that this phase itself consists of three parallel paths.…”
Section: The Npd Processmentioning
confidence: 97%
“…A dedicated expert team decides which ideas/candidates should be selected to proceed to the preliminary assessment phase (Akhilesh, 2014;Berber et al, 2013;Poetz and Schreier, 2012;Prašnikar and Škerlj, 2006;Urbig et al, 2013;Witell et al, 2011;Yan and Kull, 2014).…”
Section: The Npd Processmentioning
confidence: 99%
See 1 more Smart Citation
“…Therefore, it is important to extract effective variables associated with product development to improve performance measurement of firms. Prašnikar and Škerlj (2006) investigated the organizational and managerial factors lying behind time-to-market in four firms in Central and Eastern Europe. They presented some factors incorporated into a diagnostic framework of new product development in generic pharmaceutical companies.…”
Section: Introductionmentioning
confidence: 99%
“…Five years are generally consumed in a generic drug development. Especially, a laboratory development phase consumes around 25% from the entire development cycle [1]. Time consuming in a laboratory development phase is caused by implicit details in an original drug patent.…”
Section: Introductionmentioning
confidence: 99%