quality controls used when producing aspirin?

Answer 1

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For more info, see the link.

Answer 2

All drugs (aspirin included) manufactured in the U.S. are under strict quality control and have to be prepared under a set of guidleines called "Good Manufacturing Practices" or GMP. GMP refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act. These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing a product which is not effective or even dangerous. Failure of firms to comply with GMP regulations can result in very serious consequences including recall, seizure, fines, and jail time.

GMP regulations address issues including recordkeeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling. Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls. This provides much flexibility, but also requires that the manufacturer interpret the requirements in a manner which makes sense for each individual manuacturer.

See the links below for more info.

Rick the Pharmacist

Answer 3

You must be joking!! Making aspirin is a means to mint money and quality control, or for that matter life of fellow human beings, comes second!! this applies to pirated drugs and that Wonder drug called Viagra or cialis!!

Answer 4

http://www.answers.com/topic/aspirin-1

Answer 5

It would include sensors in the air to detect airborne concentration, proper respiratory equipment and clothing.