Education and training for medicines development, regulation and clinical research in emerging countries

dc.contributor.authorKerpel-Fronius, S.
dc.contributor.authorRosenkranz, B.
dc.contributor.authorAllen, E.
dc.contributor.authorBass, R.
dc.contributor.authorMainard, J.D.
dc.contributor.authorDodoo, D.
dc.contributor.authorDubois, D.
dc.contributor.authorHela, M.
dc.contributor.authorKern, S.
dc.contributor.authorMassud, J.
dc.contributor.authorSilva, H.
dc.contributor.authorWhitty, J.
dc.date.accessioned2018-11-15T15:30:40Z
dc.date.available2018-11-15T15:30:40Z
dc.date.issued2015-04
dc.description.abstractThe aim of this satellite workshop held at the 17th World Congress of Basic and Clinical Pharmacology (WCP2014) was to discuss the needs, optimal methods and practical approaches for extending education teaching of medicines development, regulation and clinical research to Low and Middle Income Countries (LMIC's). It was generally agreed that, for efficiently treating the rapidly growing number of patients suffering from noncommunicable diseases, modern drug therapy has to become available more widely and with a shorter time lag in these countries. To achieve this goal many additional experts working in medicines development, regulation and clinical research have to be trained in parallel. The competence-oriented educational programs designed within the framework of the European Innovative Medicine Initiative-PharmaTrain (IMI-PhT) project were developed with the purpose to cover these interconnected fields. In addition, the programs can be easily adapted to the various local needs, primarily due to their modular architecture and well defined learning outcomes. Furthermore, the program is accompanied by stringent quality assurance standards which are essential for providing internationally accepted certificates. Effective cooperation between international and local experts and organizations, the involvement of the industry, health care centers and governments is essential for successful education. The initiative shouldalso support the development of professional networks able to manage complex health care strategies. In addition it should help establish cooperation between neighboring countries for jointly managing clinical trials, as well as complex regulatory and ethical issues. © 2015 Kerpel-fronius, Rosenkranz, Allen, Bass, Demotes_mainard, Dodoo, Dubois, Hela, Kern, Massud, Silva and Whitty.en_US
dc.identifier.otherDOI: 10.3389/fphar.2015.00080
dc.identifier.urihttp://ugspace.ug.edu.gh/handle/123456789/25562
dc.language.isoenen_US
dc.publisherFrontiers in Pharmacologyen_US
dc.subjectClinical trialsen_US
dc.subjectCompetenciesen_US
dc.subjectLearning outcomesen_US
dc.subjectLow and middle income countriesen_US
dc.subjectPharmaceutical medicineen_US
dc.subjectRegulatory agenciesen_US
dc.titleEducation and training for medicines development, regulation and clinical research in emerging countriesen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Education and training for medicines development, regulation and clinical research in emerging countries.pdf
Size:
226.88 KB
Format:
Adobe Portable Document Format
Description:

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.6 KB
Format:
Item-specific license agreed upon to submission
Description: