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A D VA N C E R E G I S T R AT I O N D E A D L I N E : A P R I L 3 0, 2 0 1 0 DRUG AND MEDICAL DEVICE SEMINAR EXPERT SPEAKERS INCLUDING MAY 20 21, 2010 IN-HOUSE COUNSEL SAN FRANCISCO MARRIOTT MEDICAL
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Who needs drug and medical devices:
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Patients with chronic illnesses: Individuals with chronic illnesses often require regular medications or medical devices to manage their conditions.
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It is important to note that specific medical advice should be sought from healthcare professionals to determine the appropriate use of drugs and medical devices for individual cases.
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What is drug and medical device?
Drug is a substance used to diagnose, cure, treat, or prevent disease, while a medical device is an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article intended for use.
Who is required to file drug and medical device?
Manufacturers, distributors, importers, and packers of drugs and medical devices are required to file with the appropriate regulatory authorities.
How to fill out drug and medical device?
To fill out a drug or medical device application, companies must provide detailed information about the product, including its intended use, ingredients, manufacturing process, safety data, and labeling.
What is the purpose of drug and medical device?
The purpose of drugs and medical devices is to improve or maintain health, diagnose and treat medical conditions, and alleviate symptoms.
What information must be reported on drug and medical device?
Companies must report information such as product specifications, ingredients, manufacturing process, safety data, labeling, and any adverse events associated with the product.
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