Manufacturing
Best practices in the making of medicine are important in all aspects
which that entails: filtration needs, milling, filtering and packaging
as well the usage of compliant machinery.
Streamlining pharmaceutical manufacturing for large-scale processing
and packaging in the final phases of the cycle is critical. Incorporating
low-cost product safety and extended life cycles through improved methods
works as the foundation for innovation and continuous improvement in
pharmaceutical development and manufacturing.
Executives responsible for the largest pharmaceutical facilities in
the world will offer unparalleled insight into strategies for bringing
engineering rigor and proactive decision-making to pharmaceutical quality.
Monitoring the quality of water
Millipore Corporation’s Marilyn Romieux and Serge Ohresser look
at the benefits of a rapid microbiology detection system
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Under pressure
Contract manufacturers are being forced ? now more than ever before
? to consider their own costs.
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Talking PAT
Looking at the benefits of high-resolution ultrasonic spectroscopy as
a new process analyzing tool in PAT installation. By Evgeny Kudryashov
and Breda O’Driscoll, Ultrasonic Scientific
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Kodiak Thermal Technologies, Inc.
Transportation of temperature sensitive products is a challenge.
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Catch counterfeits using unique product codes
Counterfeit drugs are increasing in prevalence, creating some major
side effects for the pharmaceutical industry including threats to patient
safety and potentially huge financial risk.
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Counting the cost of clean air
What if I said to your HVAC engineer and your procurement personnel,
Camfil Farr will provide free HVAC filters in exchange for 50% of your
energy savings by utilizing our LCC filters!
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Technical study: Mycoplasma removal
Cell culture media is available in many different types and variations
designed to suit the specific needs of cell lines and genetically-modified
variants.
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New frontiers in drug development
While healthcare achievements in past decades have been impressive,
recent progress in genomics, proteomics, information technology and
many other fields of science and medicine should promise even greater
improvements in our lives in the years ahead, says Scott Gottlieb, Deputy
Commissioner for Medical and Scientific Affairs at the FDA.
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cGMP radiolabeling
The ultimate success of an early-stage investigational drug is difficult
to predict. In order to avoid costly late-stage clinical trial failures,
the knowledge of the pharmacological effects of an investigational drug
in the human body at an early stage has become increasingly necessary.
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galenIQ™ – the smart new choice in
pharmaceutical excipients
Description of a new non animal origin quality polyol. And evaluation
of the effects of tabletting speed, magnesium stearate concentration
and mixing time on the relationship between compaction pressure and
strength of tablets made with galenIQ™ (isomalt Ph. Eur., BP,
USP 29-NF24).
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Quality counts
Ali M. Afnan of the FDA and OPS discusses the Government?s Framework
for Innovative Pharmaceutical, Development, Manufacturing and Quality
Assurance.
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IT’s all part of the process
Process analytical technology?s future in a more agile pharma manufacturing
environment.
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Umetrics - Manufacturing Roundtable: Lay it on
the line
The PAT initiative aims, among other things, to develop processes that
ensure consistent quality of the end product, while improving efficiency
and addressing regulatory concerns.
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Clean room packaging from Bischof + Klein
Sectors such as the pharmaceutical and foodstuff industries are characterised
by innovation and continuous adaptation to current market requirements.
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Trends in pharmaceutical doors
Pharmaceutical engineers and design/build firms are challenged more
than ever to meet the needs of pharmaceutical clients.
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