Read how contributors from Genzyme, Duke Clinical Research Institute, Accenture, Oracle Health Sciences and others address some of the most pertinent challenges facing the biopharmaceutical industry including... Globalization of clinical trials driven by the need to reduce costs and recruit participants; greater outsourcing; escalating regulatory demands; increased trial complexity; and post-marketing studies. Download this paper to gain new insight into:

• Recent progress made in addressing these challenges
• Expert opinion on clinical trial management systems (CTMS) for improving trial efficiencies
• How to cut trial costs and enhance the productivity of trial participants
  

Today nearly half of all clinical trials are conducted electronically, and rising! Electronic Data Capture (EDC) technology provides industry-wide opportunities, along with challenges, that are being addressed. In this informative report industry experts and users from Pfizer, PPD, C3i and Oracle Health Sciences discuss the impact of EDC and its newest zero footprint; online iteration.  It can used anywhere, world-wide, where the Internet is available while placing greater onus on global trial support. The critical focus of this new technology is that it must support the work of the person at the heart of the clinical trial system– the investigator. Download this report to learn more about:

• Trends and Issues in an Electronic Clinical Data Management World
• The New Remote Data Capture Paradigm 
• Improving and Monitoring Clinical Data Management in the eClinical Age
• Optimizing and Supporting Remote Data Capture

Many companies have recognized that their internal business units operate as a set of business processes. These business processes are also called workflows. Modern Laboratories are highly suitable to this workflow driven approach. In fact, the lab environments successful operation is predicated on the successful definition and adherence to workflows. It could be said that a modern  laboratory is an advanced process implementing construct. It is important that laboratory management software mirrors the process driven nature of the lab thereby increasing automation, shortening learning curves, improving data quality and increasing lab throughput.

• The modern laboratory is an advanced workflow implementing construct
• Laboratory Management Software solutions should fully embrace and mirror this process driven approach
• Effective information management of workflow processes with a LIMS results in increased automation, reduced training curves, better data quality and increased lab throughput
  

High performance storage systems are a given to meet today’s life sciences R&D computational challenges. But with the explosive growth in data produced by next-gen lab equipment, scalability and long-term data management issues must also be addressed. Read this paper to learn:

• Why new lab equipment will impact R&D workflows
• How to avoid the hidden costs of long-term data management
• What approach you should take to accommodate today’s data while having the flexibility to scale to meet future demands.
  

 
Proven in the world’s most data intensive industries, Quantum StorNext is a scalable, high-performance file system which allows data sharing across Linux, Mac, Unix, and Windows operating systems and manages data in enterprise storage environments. In this Technical Brief you'll learn:

• How a high-performing file system can accelerate your business
• How to simplify your data management
• How a tiered storage approach can save you money

As a bio-technology or life sciences organization, your formulas, treatments and research and discoveries are the “lifeblood” of your business. But if you aren't protecting the integrity of your scientific data in your lab informatics systems, you risk losing IP ownership, revenue and consequently your business if you can't prove time-of-creation and data authenticity. Learn how you can implement simple, cost-effective and automated controls to protect your scientific intellectual property. Consider:

• IP protection requirements in bio-pharma and other science-oriented industries can extend out 20, 30, 40 or more years
• Most electronic lab management solutions include generic authenticity controls, so how "legally defensible" is yours?
• Only standards-compliant, independent controls can future-proof your approach to long-term IP integrity protection and authenticity.
• Learn more - get the free whitepaper now