US FDA slams second Megafine facility in India with warning letter
A second Megafine Pharma plant has landed a US FDA warning letter for cGMP violations, including sourcing API intermediate materials from a facility on import alert.
A second Megafine Pharma plant has landed a US FDA warning letter for cGMP violations, including sourcing API intermediate materials from a facility on import alert.
Almac Diagnostics will initiate sample profiling on current EORTC trials to further biomarker discovery and development.
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The Health Products Regulatory Authority of Ireland (HPRA) has said it did not recommend renewal of the GMP certificate for Wockhardt’s site in Shendra, Aurangabad.
In the absence of a CRO, the 200 patient NeoART study is relying on the UK NHS, crowdfunding and charity to trial an antimalarial generic for late stage bowel cancer.
Noramco has added cannabinoids to its portfolio of opioid APIs.
Clinerion has expanded its services into countries in Eastern Europe, the Middle East and Africa (EEMEA) following appointment of a new regional head.