Session 1: A Brief Overview of the Similarities and Differences between the US and EEC Chemical and Pharmaceutical Requirements for Clinical Trials and for the Marketing Authorization/NDA

Autor:	Roger W. Croswell
Rok vydání:	1989
Předmět:	Clinical trial medicine.medical_specialty business.industry Drug Guides Public Health Environmental and Occupational Health Alternative medicine Medicine Pharmacology (medical) Pharmacology (nursing) Session (computer science) Public relations Marketing authorization business
Zdroj:	Drug Information Journal. 23:353-353
ISSN:	0092-8615
DOI:	10.1177/009286158902300304
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::b85a40e1c1a0867593fc0d78838f8810 https://doi.org/10.1177/009286158902300304 Zobrazit plný text záznamu