India to introduce mandatory barcoding of APIs
A report showing high percentages of counterfeit drugs in India has prompted the country to introduce compulsory barcoding for APIs.
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A report showing high percentages of counterfeit drugs in India has prompted the country to introduce compulsory barcoding for APIs.
A study has shown that the majority of dermatology advisors to the FDA took payments subsequent to drug approvals.
Luxembourg and the Netherlands have been included in the mutual recognition agreement between the EU and the FDA in the US.
Emirates SkyCargo has commenced handling pharmaceutical cargo at a new purpose-built facility in Chicago.
At PQE Group we foster innovation, efficiency and quality services for sustainable regulated compliance solutions.
The Parenteral Drug Association (PDA) is excited to host its 4th Annual European Meeting.
Decreased supply of anti-rabies vaccines (ARVs) in Delhi causes outbreak of the disease.
Building from the company’s best-selling SCIEX Triple Quad™ for over 10 years, users can now get triple quad sensitivity plus QTRAP® functionality in one system.
New supercomputing centres have been selected to support Europe's researchers, industry and businesses to design medicines.
A total of 48 US states are now suing Purdue Pharma, claiming they falsely marketed their opioid drug.
A treatment for amyloidosis has been pulled from clinical trials after failing to reach endpoints.
The FDA has given its approval to a new injection for cluster headaches which reduce frequency of attacks.
The UK’s newest life sciences asset, Health Innovation Research Alliance Northern Ireland (HIRANI), has been launched at a BIO reception.
A new AI project marks the first time 10 pharmaceutical companies have agreed to share data to aid drug discovery.
The global contraceptive pill market is expected to increase to US$8.8 billion by 2024, report finds.