A company that makes a type of medicine used to treat malaria is changing the dosage, or amount, that it recommends people take. Instead of
one pill per day, the company has found that it is more effective to take two pills per day. What steps would they need to go through before they
would be allowed to change the dosage information on their package?
OA They would need to provide data to the FDA and get approval.
OB. They would need to call all the pharmacies and ask them to write the new dosage on their bottles.
OC. They would need to invite the NIH to their factory to see the process to create the pills.
OD. They would need to contact the CDC and tell them about the dosage change.

Question

23-06-2022
Health

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A company that makes a type of medicine used to treat malaria is changing the dosage, or amount, that it recommends people take. Instead of
one pill per day, the company has found that it is more effective to take two pills per day. What steps would they need to go through before they
would be allowed to change the dosage information on their package?
OA They would need to provide data to the FDA and get approval.
OB. They would need to call all the pharmacies and ask them to write the new dosage on their bottles.
OC. They would need to invite the NIH to their factory to see the process to create the pills.
OD. They would need to contact the CDC and tell them about the dosage change.

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vijayhalder031 vijayhalder031 · Answer 1 · 2022-06-29T15:49:48+02:00

Steps would they need to go through is they would need to provide data to the FDA and get approved.

The FDA or Food and Drugs Administration is a federal body or agency by the health department that regulates any approval or changes in any food or drug product.

Any change, be it change in the size, weight, color, packaging, or even the dosage of any drug is regulated by the FDA.

Everything related to the food or drug products needs a proper approval from this body.

When a pharmaceutical company need to change anything regarding the drug, maybe its packaging, dosage, mode of administration, etc; it needs to follow the FDA’s exact procedure to get it done.

It is illegal for any company to make changes in their products without the permission of FDA.

For more information about Pharmaceuticals here

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