the principle of cancer immunotherapy includes various methods of manipulations to influence immune responses against tumors in both humans and animals. this advanced technology of hybridoma production provided the necessary skills to efficiently produce highly specific monoclonal antibodies (mab). radioactively-tagged antibodies which are applied in radioimmunotherapy (rit), can target adjacen...

The Food and Drug Administration (FDA) is proposing to amend the final monograph for over-thecounter (OTC) bronchodilator drug products to remove pressurized metered-dose aerosol container dosage forms for the ingredients epinephrine, epinephrine bitartrate, and racepinephrine hydrochloride. This action is being taken because the OTC marketing of such drug products will require an approved appl...

The objective of this article is to consider the information needs of drug purchasers; whether the Food and Drug Administration (FDA) should have a role in regulating information on the characteristics and cost-outcomes impact of new pharmaceutical products to health care purchasers; and the requirements in the new FDA Modernization Act of 1997 for "competent and reliable scientific

The principle of cancer immunotherapy includes various methods of manipulations to influence immune responses against tumors in both humans and animals. This advanced technology of hybridoma production provided the necessary skills to efficiently produce highly specific monoclonal antibodies (mAb). Radioactively-tagged antibodies which are applied in radioimmunotherapy (RIT), can target adjacen...

On November 23, 2015, the US Food and Drug Administration (FDA) approved nivolumab for treatment of metastatic renal cell carcinoma (RCC), thus opening a new era immunotherapy this tumor. This review summarizes 5-year experience studying using in RCC patients.

BACKGROUND The United States (US) Food and Drug Administration (FDA) is responsible for the protection of the public health by assuring the safety, effectiveness and security of human drugs and biological products through the enforcement of the Federal Food, Drug and Cosmetic Act (FDCA) and related regulations. These enforcement activities include regulatory letters (i.e. warning letters and no...

The Food and Drug Administration (FDA) is classifying tissue culture media for human ex vivo tissue and cell culture processing applications into class II (special controls). The special control that will apply to this device is a guidance document entitled "Class II Special Controls Guidance Document: issue Culture Media for Human Ex Vivo Tissue and Cell Culture Processing Applications; Final ...

US Food and Drug Administration (FDA)-approved diagnostic assays play an increasingly common role in managing patients to prolong lifespan while also enhancing quality of life. Diagnostic assays can be essential for the safe and effective use of therapeutics (companion diagnostic), or may inform on improving the benefit/risk ratio without restricting drug access (complementary diagnostic). This...

Submit Manuscript | http://medcraveonline.com Abbreviations: PMMA: Poly Methyl Methacrylate; HEMA: Hydroxyethyl Methacrylate; FDA: Food and Drug Administration; BCLA: British Contact Lens Association; ACHIEVE: Adolescent and Child Health Initiative to Encourage Vision Empowerment; UDVA: Uncorrected Distance Visual Activity; IOL: Intraocular Lens; IOP: Intraocular Pressure; MEMS: Micro Electro M...

background adulterated herbal weight loss products with containing undeclared synthetic drugs are common and responsible for many serious health damages. objectives the purpose of the study was to determine five synthetic adulterants in eight common herbal weight loss supplements, which are currently sold in iran markets, to verify their presence in supplements, without mentioning on the labels...