Design and Bioanalysis of Peptide-Drug Conjugate (PDC)
PDCs are primarily composed of three parts—peptides, linkers, and cytotoxic payloads.
PDCs are primarily composed of three parts—peptides, linkers, and cytotoxic payloads.
The 510(k) is a complex application to the FDA, because the application is to demonstrate that the device is safe and effective, and it is equivalent to another device which is on the market.
FDA medical device registration is required for all medical devices marketed in the United States, ensuring that they meet the safety and efficacy standards set by the FDA.
Protheragen-ING Lab, a well-known and reputable Good Laboratory Practices (GLP) service provider, has recently unveiled its cutting-edge medical device services.
Protheragen-ING's veterinary products are designed to meet the specific nutritional needs of different animals, including livestock, poultry, and pets.
In exciting news, Protheragen-ING officially become a member of the Drug, Chemical & Associated Technologies (DCAT) Association.
The hydrogel microneedle patch consists of a patch with tiny microneedles made of hydrogel, which can deliver drugs directly into the skin.
In recent years, microneedle patches have emerged as a revolutionary technology in the beauty and skincare industry.
The development of oral thin films has gained significant traction in the pharmaceutical industry due to their ease of use, quick disintegration, and improved bioavailability.
In the field of pharmaceutical science, stability analysis plays a crucial role in ensuring the safety and efficacy of pharmaceutical products.
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