Results 61 to 70 of about 27,977,136 (206)

Evaluation of the Pharmaceutical Industry Investment Program [PDF]

With the expiry of the Pharmaceutical Industry Investment Program (PIIP) in 2004, the Commission was asked to conduct an evaluation of the program’s rationale, effectiveness and efficiency. The study commenced in August 2002.
Productivity Commission
core  

Has the European Union Achieved a Single Pharmaceutical Market? [PDF]

This paper explores price differences in the European Union (EU) pharmaceutical market, the EU's fifth largest industry. With the aim of enhancing quality of life along with industry competitiveness and R&D capability, many EU directives have been ...
Gabriel Picone, Aysegul Timur, Jeffrey S. DeSimone   +2 more
core  

An NLP-based technique to extract meaningful features from drug SMILES

iScience
Summary: NLP is a well-established field in ML for developing language models that capture the sequence of words in a sentence. Similarly, drug molecule structures can also be represented as sequences using the SMILES notation.
Rahul Sharma, Ehsan Saghapour, Jake Y. Chen   +2 more
doaj   +1 more source

Permeability of frog skin to chemicals: effect of penetration enhancers

Heliyon, 2019
Rarely do commercial chemical products contain solely the active chemical/ingredient. It is therefore important to consider whether ingredients other than the active may: 1) alter absorption of the active chemical, or 2) be absorbed themselves, resulting
Victoria K. Llewelyn, Lee Berger, Beverley D. Glass   +2 more
doaj   +1 more source

The Future of Pharmaceutical Manufacturing Sciences

Journal of Pharmaceutical Sciences, 2015
The entire pharmaceutical sector is in an urgent need of both innovative technological solutions and fundamental scientific work, enabling the production of highly engineered drug products. Commercial-scale manufacturing of complex drug delivery systems (DDSs) using the existing technologies is challenging.
Rantanen, Jukka, Khinast, Johannes
openaire   +3 more sources

Scientific basis of the development and standardization of herbal medicines

Регуляторные исследования и экспертиза лекарственных средств, 2018
The present paper conceptually considers scientific approaches to standardization of starting materials of herbal origin and herbal medicinal products.
I. A. Samylina, V. A. Kurkin, G. P. Yakovlev   +2 more
doaj  

R&D Portfolios and Pharmaceutical Licensing [PDF]

We examine how R&D portfolios of drug pipelines affect pharmaceutical licensing, controlling firm size, diversity, and competitors in R&D and product markets.
Junichi Nishimura, Yosuke Okada
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Application of hydrophilic interaction liquid chromatography for the quantification of succinylcholine in Active Pharmaceutical Ingredient and medicinal product. Identification of new impurities of succinylcholine chloride

Heliyon, 2018
A new method, using hydrophilic interaction chromatography (HILIC), for quantification of succinylcholine and impurities in Active Pharmaceutical Ingredient (API), as well as in the medicinal product, was developed.
Arkadiusz Szterk, Adam Zmysłowski, Shela Gorinstein   +2 more
doaj   +1 more source

The regulation of Pharmaceutical Excipients [PDF]

, 2016
Pharmaceutical excipients are vital components of drug formulations and are generally considered pharmacologically inert. Control of excipient manufacturing and distribution is now considered a key priority by regulatory authorities and pharmaceutical ...
Vikrant Saluja, Bhupinder Singh Sekhon
core  

Proportionality between powder cohesion and unconfined yield strength from shear cell testing

Heliyon, 2019
From an analysis of the geometry of the yield locus and the Mohr's circle for determining unconfined yield strength (fc) in shear cell testing, it has been shown that powder cohesion is proportional to fc, where the proportionality constant is a function
David J. Sun, Changquan Calvin Sun
doaj   +1 more source