Pakistan’s drug regulator has come up with a strategy to ensure uniformity in how pharma and medical device companies disclose the money they spend on doctors and medical institutes under new ethical marketing rules.
The Drug Regulatory Authority of Pakistan is taking steps to ensure that drug and medical device companies follow a harmonized approach when it comes to disclosing the expenses they incur every year as part of their product marketing activities involving health care professionals and medical institutes.
Companies are required to make such disclosures to the DRAP and relevant tax authorities under the “Ethical Marketing to Healthcare...
The US FDA Commissioner pushed for a rebalancing of the US’s pharmaceutical supply chains while also stressing that there is a role for US-China commerce that would be risky to compromise.
A total of 748 key medicines are now affected by the four-month stock requirement, compared with 422 in 2021.
The UK regulator approved 16 medicines containing a new active substance in the first half of this year, while the European Commission issued marketing authorizations for 20 NAS-containing drugs.
Revised recommendation is based on most recent data on circulating strains in US, where KP.3 is now dominant. Novavax sticks with plans targeting the JN.1 ‘parent strain.’
Pink Sheet reporter and editors discuss the US FDA’s changes to the COVID-19 vaccine indication and its revocation of the vaccine emergency use authorizations, as well as new vaccine coverage and reimbursement questions.
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