Drug Device Articles & Analysis
12 articles found
This could revolutionize the field of organ transplantation and offer hope to patients with organ failure. Drug testing: Bioprinted tissues can be used to test new drugs and therapies in a more realistic and humane way than traditional animal models. ...
ByMatexcel
Factors Considered When Determining Shelf Life Expiration Dates Shelf life expiration dates are vitally important to ensure medical devices are safe to use. The Food and Drug Administration (FDA) requires product labels to indicate an expiration date if a certain component is not useful past a certain date. Therefore, medical device ...
Coated Microneedles Coated microneedles are also known as surface drug-loaded microneedles. The drug is attached to the surface of the microneedle by infiltration, coating or drug loading outside the needle. ...
SMC Group provides an end-to-end solution for sterile injection devices, including autoinjectors. This end-to-end solution includes customisation of the appropriate device platform to meet the specific user requirements, component manufacture, filling of the primary drug container, and assembly and integration to produce the final ...
Alucent Biomedical Inc. is rethinking peripheral artery disease (PAD) treatment with a novel natural scaffolding technology based on a light-activated drug therapy delivered via a balloon catheter. This first-of-its-kind drug-device therapy, known as Natural Vascular Scaffolding (AlucentNVS), is designed to provide a more natural and effective ...
Early Diagnosis is Essential Q: What is the benefit of an early AMD diagnosis if there’s not yet an FDA-approved drug to treat it? Dr. Dierker: We are fixated on a stage of disease that optometrists can’t do much about (i.e., advanced AMD) instead of taking a hard look at the statistics and asking what we could be doing to turn things around for our patients before ...
Hundreds of millions of Americans rely on life-saving and sustaining medications and medical devices every day. Ensuring the drugs and devices that they depend on are not contaminated is critical for the health of the country, and the responsibility of the U.S. Food and Drug Administration (FDA). To address safety concerns in ...
It comprises of hospitals, medical devices, telemedicine, clinical trials, medical equipment, integration of health insurance and boom of medical tourism. ...
Auto-injectors, drug delivery medical devices that automatically administer an injectable dose for a patient, have grown in popularity over the past decade. ...
Noxilizer has developed an optimal sterilization process specifically for prefilled syringes and other drug-delivery devices. The low temperature NO2sterilization process will effectively sterilize the external, gas accessible surfaces of the syringewith minimal to no impact on the contents of the syringe. ...
Section 6002 of the Affordable Care Act (ACA) of 2010 – also known as the Physician Payments Sunshine Act (PPSA) – requires all manufacturers of drugs, medical devices and biologicals that participate in US federal healthcare programs to disclose any and all payments or other transfers of value made to physicians or teaching hospitals. ...
Abstract: The FDA has issued a draft guidance document on how manufacturers should present risk information in promotional material and ads for prescription drugs and medical devices. It describes the factors that the agency takes into consideration when evaluating ads and promotional labeling for prescription drugs and medical ...