Thursday, September 01, 2011
Effectively managing biospecimens along with their associated data are key components of efficient clinical development.
Thursday, September 01, 2011
Safety studies are required for all drugs undergoing testing in pediatric patients. While efficacy can be extrapolated in some cases on the basis of adult studies, safety studies must be separately conducted in pediatric patients.
Thursday, September 01, 2011
The market for biopharmaceuticals continues to expand in both volume and revenue.
Tuesday, November 01, 2011
The Extractables and Leachables Safety Information Exchange (ELSIE), a consortium of pharmaceutical, biotech, and medical device companies has developed a database that will hold (i) safety information on extractables and leachables from a variety of...
Tuesday, November 01, 2011
Pediatric research is ethically challenging, requiring protection of children from potentially harmful exposure while encouraging drug development and pediatric labeling.
Tuesday, November 01, 2011
Patheon is a contract development and commercial manufacturing company that focuses on the drug product.
Tuesday, November 01, 2011
Currently providing quality, integrity and performance in contract manufacturing, product development, formulation, fill / finish, lyophilization and analytical services for both vial and syringe applications, PYRAMID Laboratories, Inc. maintains a ...
Why should pharmaceutical companies consider outsourcing laboratory
services, particularly in today’s uncertain economic times?
Latin American (LA) countries operate increasingly in accordance
with international standards and guidelines. This has been a major
driver for increasing interest and placement of clinical studies
in the region.
Managing research and providing the right structures to allow
innovation to flourish is not trivial.