Clinical Trial Services

Nov 06, 2013
By Pharmaceutical Technology Editors
ISPE’s survey is industry’s first large-scale effort to collect data on patient experiences with clinical trial materials.
May 02, 2012
PTSM: Pharmaceutical Technology Sourcing and Management
Clinical research organizations see reform in clinical-trial process, including the establishment of chief innovation officer at FDA.
Oct 02, 2011
Pharmaceutical Technology
By Pharmaceutical Technology Editors
The authors examine risk management relating to the quality issues of clinical-trial materials and discuss areas that would benefit from additional consideration and harmonization.
Feb 01, 2011
Pharmaceutical Technology
By Pharmaceutical Technology Editors
The author analyzes the results of a survey that polled pharmaceutical executives and managers about both sides of the outsourcing relationship. Read this and other preferred organization articles in this special issue.
Oct 01, 2010
Pharmaceutical Technology Europe
The FDA has issued a final rule that clarifies what safety information must be reported during clinical trials of investigational drugs and biologics.
Aug 01, 2010
Pharmaceutical Technology
As emerging markets become increasingly important for the pharmaceutical majors, companies are re-evaluating their outsourcing strategies. This article is part of the 2010 Outsourcing Resources special issue.
Jul 22, 2010
ePT--the Electronic Newsletter of Pharmaceutical Technology
By Pharmaceutical Technology Editors
Pfizer Ends Second Tanezumab Clinical Program; Catalent VP Joins USP Panel; And More.
Jun 02, 2010
Pharmaceutical Technology
CROs and CMOs adapt their business models and capabilities to meet sponsor companies' need to reduce costs and accelerate development time.
Jun 01, 2010
Sponsored Content
By Pharmaceutical Technology Editors
From product development to finished patient kits, Rockwell Automation equipment is used throughout the entire process.
Mar 01, 2010
Pharmaceutical Technology
By Pharmaceutical Technology Editors
The author examines the use and advantages of disposable technologies in the fill–finish of sterile pharmaceutical products and how these technologies can reduce costs and time in producing clinical-trial materials.
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