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A mandatory, enforceable code for ethical pharmaceutical marketing is required. The recent controversy over a specific brand of the painkiller paracetamol 650 mg tablet is more about the unethical marketing tactics of India’s pharmaceutical industry.
The inclusion of QR codes on APIs that are produced in India or imported and distributed is required by the Indian government in order to make it easier to track and trace the products throughout the supply chain.
Alembic Pharmaceuticals reported that from August 18 through August 30, 2022, the US Food and Drug Administration (USFDA) inspected the drug manufacturer’s injectable facility (F-3) in Karkhadi.
Aurobindo Pharma announced plans to invest close to Rs 300 crore in the capacity expansion of biologics manufacturing facilities through its wholly owned subsidiary, CuraTeQ Biologics.
The proposals from the three states- Himachal Pradesh, Gujarat, and Andhra Pradesh- under the Scheme for the “Promotion of Bulk Drug Parks, ” a program to aid in the nation’s drug manufacturing, have received “in-principle” approval from the Dept. of Pharmaceuticals.
US Food and Drug Administration (FDA) has approved Xenpozyme (olipudase alfa-rpcp) for the treatment of non-CNS manifestations of acid sphingomyelinase deficiency (ASMD) in adults and children.
A trial that was set to start next week has been
postponed thanks to Johnson & Johnson’s
decision to pay $40.5 million to resolve New
Hampshire’s claims regarding the pharma
company’s contribution to the nation’s opioid
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