Clinical, Medical & Diagnostic Products
Liquid Handling Products for Faster Diagnostic Testing and Research
Integra Biosciences’ cost-effective liquid handling products are ideal for molecular diagnostics workflows, particularly during the COVID-19 crisis, making it easy for labs to scale up their testing capacities quickly and easily.
It is often assumed that high throughput can only be achieved with huge investment. This simply isn’t the case with Integra’s affordable pipetting solutions, which can increase lab productivity and the reproducibility of results, without the need for large liquid handling platforms and at an affordable price.
Integra instruments can easily be implemented into any lab’s workflow, meeting a wide range of throughput needs simply by replicating the workflow on multiple cost-effective workstations running in parallel. This provides scalability without complexity, and each workstation’s compact footprint ensures efficient use of lab space, as well as allowing them to easily fit in biosafety cabinets for safe handling of hazardous samples.
All Integra systems are shipped fully assembled to minimise set-up time. Combined with intuitive operation, this allows labs to get their workflows up and running - from unboxing to the first run - within minutes.
More information online:
ilmt.co/PL/oL20 53437pr@reply-direct.com
Enhanced Features Added to Clinical Supplies Labelling Platform
Based upon its collaborative work with three leading pharmaceutical companies, PRISYM ID has launched an update to its flagship software solution for clinical supplies labelling. Enhancements to PRISYM 360 include the automation of booklet production with improved regulatory rules and language management and a new compliance-friendly product - the 3-Step Clinical Label Print Process.
The update is part of PRISYM ID’s continued responsiveness to the needs of organisations undertaking clinical trials. Clients are seeking to leverage the latest technology improvements to be able to quickly launch studies in multiple countries at the same time, while building in flexibility to allow for subsequent drug dosage or administration changes. They need processes which are fully auditable, are logged and that offer traceability for every printed label or booklet.
The 3-Step Clinical Label Print Process encapsulates industry best practice, significantly reducing the possibility of individual user error when printing single page labels. It will not let the same person raise and approve labels, it ensures a test label is printed and stored electronically, prints test labels with a watermark, and creates summary reports and audit trails.
New content management controls are designed to merge the right rules and phrase content together for particular drugs and protocols, and ensure they are produced in the right languages for the countries in which trials are run. They can replace email and disparate, clunky systems that have manual steps and are liable to user error.
Simon Jones, Vice President of Product Marketing, said: “We have worked closely with three key customers who explained to us their challenges in quickly creating multi-page booklets for studies in 40+ countries, especially where participating countries have specific regulatory requirements in respect of language, indications, warnings, precautions, and symbols.
“This update is therefore all about clinical trial functionality enhancements which streamline the process of creating a label or a booklet and getting clinical trials started more quickly. Our 3-Step Clinical Label Print Process eliminates errors, risks and ensures full accountability.”
More information online:
ilmt.co/PL/5aV6 52624pr@reply-direct.com
Swabs for COVID-19 Testing
In order to meet the required capacity of 100,000+ COVID-19 tests per day, the Government guidelines on transport swabs has made allowances for Laboratories to use alternatives to Viral Transport Medium (VTM), subject to local validation.
The broad range of swabs available from Alpha Laboratories Ltd is helping to support this demand. The swabs are ideal for collecting and transporting virological, bacteriological, serological and cytological samples. Swabs that are CE marked for IVD, conform to the MDD 93/42/EEC for Class IIa.
Alpha Laboratories’ swabs are available in various packaging formats, from bulk packs that are ideal for diagnostic kit assembly, to single swab peel-packs that are perfect for POC testing. They are manufactured in ISO class 8 or higher clean room conditions, under an ISO 13485 accredited quality system. They are certified free of PCR inhibitors, human DNA, RNase, DNase and pyrogens. Where swabs are marked as sterile this is by irradiation or EtO.
More information online:
ilmt.co/PL/LpAw 52376pr@reply-direct.com
The Spotlight could be on you! Contact Gwyneth Astles on +44 (0)1727 855574 or email:
gwyneth@intlabmate.com
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