Safety/Efficacy White Papers & Case Studies
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Switching EDC Platforms To Rescue In-Flight Clinical Trials
5/7/2013
The decision to switch an EDC platform for in-flight trials is not easy and is fraught with risks. A majority of companies continue to plough forward with higher costs and operational pains due to a failing EDC platform. Read this white paper and learn how Acceliant's low-risk EDC migration can deliver legacy EDC retirement, lower operating costs, and peace of mind for all teams working towards the success of a clinical trial. By Ven Thangaraj, CTO, Acceliant
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New Molecular Entities (NMEs) - The Path Of Resistance
5/3/2013
On a global scale, the number of new molecular entities (NMEs) in development—and, more importantly, the number being approved by regulatory authorities— has dropped significantly in recent years.
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Global Pharmacovigilance And Safety Solutions
4/23/2013
As the world’s largest privately held provider of global communication and technology solutions to the life sciences industry, TransPerfect offers an end-to-end solution to handle all aspects of pharmacovigilance and safety management in over 170 languages.
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Overcoming Clinical Challenges In Metabolic And Cardiovascular Disease With Metabolomics
4/10/2013
Metabolic diseases (e.g. obesity, type 2 diabetes, and hypertension) are a rapidly expanding health care concern. Although there is a high demand for novel therapies, the challenges are substantial as existing drugs typically fail due to lack of efficacy or safety, and clinical studies often extremely large and protracted.
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Overcoming Clinical Challenges In Oncology With Metabolomics
4/10/2013
Cancer continues to be a formidable disease with an overall success rate of bringing new drugs to market of only 5-8%.
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Improving Life Science Operations With Digital Signatures eBook
2/27/2013
Today, 8 of the top 10 pharmas and 6 of the top 10 CROs use ARX’s CoSign® digital signature solution to help them benefit from fully electronic regulatory document lifecycles, compliance with various FDA GxP regulations, and efficiency in supporting audits.
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eTMF And The eClinical Universe
2/21/2013
How Electronic Trial Master Files (eTMFs) Work With Other eClinical Systems To Help You Meet Regulatory Requirements.
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Brochure: Norwich Clinical Services
2/1/2013
Norwich Clinical Services is a contract research organization that provides Bioanalytical Services, Pharmacovigilance and Clinical Research Programs to the pharmaceutical and biotech industries.
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Phase II Primary Insomnia Program In Need Of Full-Service CRO Management
12/6/2012
Clinilabs, a contract research organization (CRO), was selected by an international drug discovery and development company to provide full-service CRO management of a phase II primary insomnia program.
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PiKo® Monitors Brochure
4/27/2012
Ideal for clinical trials, PiKo® Lung Health Monitors deliver lung function measurements not traditionally available through home monitoring.