anonymous
Guest
anonymous
Guest
Curious on your thoughts.
Working for a company that potential created a product shortage for a patent ending drug (drug A) to help force hospitals to quickly review and add a second, non patent expiring drug (drug B) to formulary.
To help with expediting reviews, the company canceled all contracts on drug A, basically doubling the cost and trying to promote drug B as a similar yet cheaper option. However, while the cost of drug B verses drug A is cheaper today, that is not true compared to what drug A was priced at prior to canceling the contracts.
Just curious to what extent the FDA would be interested in this sort of potential unethical behavior?
It’s just tough facing customers when most of us feel like this was not the most ethical way to treat long standing customers.
Appreciate any insights.
Working for a company that potential created a product shortage for a patent ending drug (drug A) to help force hospitals to quickly review and add a second, non patent expiring drug (drug B) to formulary.
To help with expediting reviews, the company canceled all contracts on drug A, basically doubling the cost and trying to promote drug B as a similar yet cheaper option. However, while the cost of drug B verses drug A is cheaper today, that is not true compared to what drug A was priced at prior to canceling the contracts.
Just curious to what extent the FDA would be interested in this sort of potential unethical behavior?
It’s just tough facing customers when most of us feel like this was not the most ethical way to treat long standing customers.
Appreciate any insights.