samedan logo
 
 
spacer
home > epc > autumn 2004 > developments and trends in lims - a 'coming of age'?
PUBLICATIONS
European Pharmaceutical Contractor

Developments and Trends in LIMS - A 'Coming of Age'?

Over the last 10 years, laboratory information management systems (LIMS) have changed beyond recognition. Increased regulatory requirements have meant that much more data is now being recorded; data that must be turned into useful information that is immediately available across the enterprise. This leverages operational excellence by allowing rapid business decisions based on better information, driving up efficiency whilst reducing costs. New technologies have facilitated the extension of the LIMS outside the traditional confines of the laboratory, providing deployment options that allow remote access from satellite laboratories, field workers, customers and so on. This has meant that the LIMS can truly be considered an enterprise level business system, with the capability to be deployed globally, irrespective of different time zones or local languages.

All this has meant that the modern LIMS is designed to be much more flexible than its predecessors were. This flexibility can take several forms. A modern LIMS makes extensive use of workflows that can be easily configured to match existing business processes, meaning that a LIMS implementation no longer requires that these processes must be re-engineered. Workflows determine the steps that define the sample life cycle, including batch release. They also cover supporting processes such as specification review and release. Workflows also define the testing procedures, which may consist of multiple, non-linear steps.

Each step may involve the recording of data, and the result for a given step may determine which of several possible next steps should be performed. In earlier systems, typically only the final outcome of the test was recorded in the LIMS; in modern systems, the LIMS leads the operator through the defined steps making appropriate recommendations based on the entered results, the raw data or a resource reference. This leads us to another development in LIMS: the increased capability of recording business logic within the system, where it can be automated, rather than within procedures that must be manually implemented.


Read full article >>

Rate this article You must be a member of the site to make a vote.  
Average rating:
0
     

There are no comments in regards to this article.

spacer
By Stefano Marocco, Account Manager and Elian Winstanley, Managing Director at STARLIMS, UK

Stefano Marocco is an Account Manager at the UK STARLIMS office. Primarily an expert in LIMS implementation, he offers advice on how to develop time- and cost-effective solutions that optimise automation of laboratories' operations, and ways to manage samples in an environment that complies with regulatory requirements. Stefano holds an honours degree in Business Studies from South Bank University, London. He has over five years' experience in the LIMS industry, particularly in the pharmaceutical sector, gained with various solution providers.


Elian Winstanley has been involved with LIMS since the early 1990s. He has led teams who have successfully implemented LIMS for clients in a wide variety of market sectors including pharmaceutical, environmental monitoring, chemical manufacturing, food and beverage and contract laboratories. After graduating from Manchester University with a joint honours degree in Pharmacology and Physiology, followed by a masters in Physiology, he worked as a Liquid Chromatography and Data Systems specialist for a major laboratory instrument supplier before moving to laboratory information management. He currently manages the UK STARLIMS office.


spacer
Stefano Marocco
spacer
spacer
spacer
Elian Winstanley
spacer
spacer
Print this page
Send to a friend
Privacy statement

Industry Events

4th Annual Patient Recruitment and Retention in Clinical Trials

13-15 October 2008, Amsterdam

Patient recruitment is now consuming thirty percent of clinical trial time - more time than any other clinical trial activity - and almost half of all trial delays result from patient recruitment problems. As the recruiting culture becomes more sophisticated and the forces affecting patient enrollment grow more numerous and complex, pharmaceutical companies are striving to discover new strategies to facilitate enrollment in clinical trials. With increasing industry pressure to develop, test and market greater numbers of new drugs faster, pharmaceutical companies need to perform clinical trials as quickly as possible. Inefficient patient recruitment processes is a formidable barrier to pharmaceutical companies' success in launching new products. Improving the patient recruitment process is imperative to avoid wasted investments and eliminate costly delays in bringing new drugs to market -- today and even more so in the not-so-distant future. Improved patient recruitment presents one of the largest opportunities for pharmaceutical companies to eliminate delays in clinical trials, thereby making it possible to reduce time to market.  With patent time limits and large overheads meaning that any delays in the development timeline can be disastrous, a good understanding of how to successfully recruit patients for trials is vital for any company looking to succeed.
More info >>

 
News and Press Releases

MipTec, October 14 – 16, 2008, Switzerland

MipTec about to take off by joining forces between Life Sciences Week, ALL-SystemsX.ch-Day, & Jobvector.com    
More info >>

 

©2000-2007 Samedan Ltd.
About Us | Register | Login | Site Map | Terms and Conditions | Contact Us |
Add to favourites

Print this page

Send to a friend
Privacy statement