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Public consultation on key principles for ePI of EU medicines
The European Medicine Agency has launched a six month consultation on the principles that will form the basis of the electronic product information (ePI)...
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Manufacturing
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Growing role of personalised and precision medicine in cancer treatments
The role of personalised and precision medicine may be ideal for the treatment of cancer, but questions about consequences and society issues still remain...
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FDA approval for leukaemia non-chemo combination therapy
The FDA has approved the first ever non-chemotherapy combination treatment using ibrutinib and obinutuzumab for the most common form of adult leukaemia...
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Implementing the Falsified Medicines Directive
Implementation of the Falsified Medicines Directive is an important step in order to help prevent fraud in the pharmaceutical industry...
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Price disclosure legislation ‘not likely to lower drug costs in the US’
Trump's administration has recommended that drug prices are widely advertised to help push prices down - but a study has shown that the scheme may not work...
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Lithium treatment and GKS3 suppression could lead to kidney failure
Researchers have warned that certain psychiatric medications and treatments for bipolar disease could lead to the development of kidney failure...
whitepaper
Flyer: Sterile manufacturing – finished dosage forms
Eurofins CDMO provides a wide range of aseptic processing services for all drug product configurations with flexibility to accommodate a wide range of compounds, primary packaging systems, batch sizes and fill volumes to help develop your Active Pharmaceutical Ingredient or bulk product into Finished Dosage Forms for use in clinical…
webinar
Annex 1 Revisions: Let’s talk TOC and conductivity requirements for pharmaceutical water systems
22 January 2019 | By SUEZ
Register for our latest webinar on the proposed Annex 1 revision on pharmaceutical water to prepare for future compliance...
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Computer programme that could bypass patents to produce synthetic drugs
Software that can bypass current intellectual property and design medication with the same function as top drugs could help pharma companies...
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The Falsified Medicines Directive: steps to compliance
As the date of implementing the FMD comes closer, organisations need to be ensuring compliance, whether in the EU or even after a possible no-deal Brexit...
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NewAge® Industries celebrates its 65th anniversary
NewAge Industries has reached another significant event in its history: 2019 marks the company’s 65th year in business...
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Developing the production of the radioisotope Tc-99m within the US
A team of university researchers have collaborated together to develop a method to produce the radioisotope Tc-99m in the US to prevent having to import it...
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Further scandal for China’s pharmaceutical industry
Chinese police say they have opened an investigation into reports that at least 145 children received an expired polio vaccine...
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Diversifying drug development with a metal catalyst
Researchers have outlined a method of formulating drug-like aliphatic and aromatic carbon-hydrogen scaffolds into drugs using a metal catalyst...
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Polish researchers develop method to recycle pharma packaging
The development of a process to recycle pharmaceutical waste products has led to the recovery of aluminum and polyvinyl chloride (PVC) from blister packs...
