BIOTEC INTRODUCES PRISYM MEDICA LABELLING SYSTEM
Biotec has introduced a new labelling system to its clinical trials process to help manage label production, increase efficiency and reduce costs to clients.
The PRISYM Medica Labelling Software, which supports compliancy with both EU and US regulatory requirements including FDA and GMP, has a flexible label design feature to allow the input of variable data per production run and access to stored information for label reprints.
Rachel Griffiths, Operations Director, said, “The new labelling system has a number of important benefits which will help us to be more time efficient, reduce wastage, reduce the risk of errors and allowed us to access archived data more easily. The system also allows Biotec to design and print a large variety of labels in-house, including tear-off & wrap-around labels, without the need to outsource resulting in shorter lead times and a significant cost saving”.
“We have been operating with the system since July 2009 and have already noticed the difference in our time efficiency and costs. We are delighted to have trialed the new system and are extremely pleased with the results.”
Benefits of the PRISYM Medica labelling solution is that one system manages the complete labelling process including label design, review, approval, reprint and reconcile functions. It also includes purpose built user security, group security and secure audit logging to ensure complete peace of mind.
Dave Taylor, Product Manager at PRISYMID said, “The PRISYM Medica Labelling System is purpose designed to support our customers to be FDA and GMP compliant which makes it an attractive proposition for clients such as Biotec. It s ideal for securely and accurately managing clinical trials data for supplies and complete patient pack labelling. We're thrilled with the results being achieved by Biotec so far, and are looking forward to continuing this successful working relationship in the future.”
Biotec is a UK based Clinical Trials Supply company specialising in the import, qualified person certification, labelling, assembly, storage and worldwide distribution of clinical trial supplies for Phase I to Phase IV trials including temperature sensitive biopharmaceuticals. The company has a number of international clients for which they handle products that need to be maintained at extreme temperatures.
For further information please contact Fiona Withey at Biotec on 01656 750550 or email Fiona.withey@biotec-uk.com or visit www.biotec-uk.com. For further information on the new Prisym Labelling System please contact Holly Purchase at PRISYMID on 0118 9364403 or email hollypurchase@prisymid.com or visit www.prisymid.com
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