Srichakra receives European Food Safety approval for its food-grade recycled rPET
Srichakra receives European Food Safety approval for its food-grade recycled rPET
Srichakra receives European Food Safety approval for its food-grade recycled rPET
The single in vitro diagnostic test helps inform therapy decisions according to clinical guidelines to enable precision medicine earlier in the disease journey
Feedback and remarks of the industry and stakeholders are invited till the 25th of March 2022
It is only the second generic application approved by the USFDA
Macitentan tablets, 10 mg have an estimated market size of US $ 797 million for twelve months ending Dec 2021 according to IQVIA
In numerous neurological and rare disorders, where clinical characteristics can be confusing, NGS-based approaches have demonstrated considerable increases in disease detection rates over other approaches
Amit Jaju, Senior Managing Director, India in an interview with Thomas C Thottathil outlined the steps Indian pharma companies should follow to be compliant with global regulatory requirements
Digital meetings driving international partnering at CPhI Japan as companies search for ingredients suppliers
Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers releases guidelines for the scheme
Casimir further differentiates Emmes’ industry-leading rare disease research capabilities
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