Wonderware has launched software to improve the management of batch processes, offering users the ability to easily install additional processing lines or manufacturing cells.
With big pharma continually seeking greater efficiency, improving QA/QC to reduce wastage and avoid costly recalls has become increasingly important, a fact that Mettler Toledo hopes will win the latest generation of its FreeWeigh.Net software an industrial...
A leading software provider to the life science industry has formed
an alliance with a specialist supplier of radio frequency
identification (RFID) printing and bar code labelling hardware to
offer dedicated solutions to pharma, biotech...
IDBS look to speed up laboratory research by enabling more
efficient knowledge transfer with its latest electronic lab
notebook (ELN) suite, E-WorkBook 7.0.
The Food and Drug Administration (FDA) is expected to issue a
revised version of its regulation on electronic signatures and
records by the end of the year, which will force drug and device
companies to reconsider their current information...
Italian pharmaceutical dosing and packaging equipment manufacturer,
MG2, has launched two new dosing machines for hard gelatine
capsules, which can handle different dosing combinations in the
same capsule, such as powder and tablet,...
Metrohm has launched a new generation of its Capsule and Tablet
Analysis System (CTAS), a unit designed specifically for making and
testing solid dosage samples, claiming the system saves laboratory
personnel time as well as improving...
Schneider Electric has teamed up with automated handling company
PES Technology to develop a bespoke packaging line for a hazardous
and time-critical pharmaceuticals process.
Germany's L B Bohle, a specialist in dispensing, granulating and
milling equipment, has introduced a new granulator for
pharmaceutical applications that allows for continuous throughput
of materials.
3M has launched an updated version of its Integrated Packaging Tool
software that brings it into compliance with the US Food and Drug
Administration's 21 CFR Part 11 regulations on electronic
record-keeping, used to generate...
The US Food and Drug Administration is planning to hold a meeting
in June to re-examine its regulations on electronic records and
signatures, used to generate the audit trail in the food and drug
industries, to examine whether some...
UK tablet press and coating machine specialist Manesty will
introduce another product in its Xpress range at the TOTAL 2004
show next month as it navigates the sea-change in its business that
has emerged over the last few years.
Tecan of Switzerland's US subsidiary has launched Cellerity, a new
system designed to produce a ready supply of cells for cell-based
assays, at the LabAutomation 2004 exhibition, which opened its
doors yesterday.
Ireland's QUMAS has said it will launch its latest regulatory
compliance product, QUMAS Visa, at the 39th Annual Meeting of the
Drug Information Association in San Antonio, Texas, 15-19 June.
