Luminex has received approvals from the US Food and Drug Administration (FDA) and EU authorities for the new version of xTAG CYP2D6 (Cytochrome P450 2D6) Kit. An IVD assay, the xTAG CYP2D6 Kit analyses a patient's CYP2D6 genotype from ...
Kush Bottles, a distributor of medical grade containers, has launched a new line of child-resistant, made in US containers to securely store medication safely. Meeting the standards of child-resistant packaging, the new Kush containers ...
US-based pharmaceutical grade containers distributor Kush Bottles has launched a new line of BPA-free child-resistant containers. Claimed to the better choice for an easy, convenient and secure way to store medication safely, the new Kush ...
The USFDA has cleared Actavis' abbreviated new drug application (ANDA) for Lamotrigine orally disintegrating tablets, 25mg, 50mg, 100mg and 200mg. A generic version of GlaxoSmithKline's Lamictal ODT, the antiepileptic drug is indicated ...
How do you use packaging to communicate your sustainable strategy to customers? Come and find out. On July 17, 2013, Jim Hanna, director, environmental impact, Starbucks Coffee Co., will speak at the Packaging Digest Global Food & ...
Tags: Packaging, Sustainability, Gateway
Olde Thompson is recalling 1,075 cases of Earth’s Pride Organics Organic Oregano packed in 2.2oz. glass jar due to possible contamination by Salmonella, according to the US Food and Drug Administration (FDA). The recall affects ...
Specialty pharmaceutical company Actavis has won FDA approval for abbreviated new drug application (ANDA) of generic equivalent to Endo Health Solutions' Opana ER. Oxymorphone Hydrochloride extended-release tablets, which is available in ...
Tags: FDA, ANDA, Generic Opana ER
The US Food and Drug Administration (FDA) has cleared Boehringer Ingelheim's tyrosine kinase inhibitor Gilotrif (afatinib) as a new medication for patients with late stage (metastatic) non-small cell lung cancer (NSCLC). The approval also ...
Tags: FDA, Lung Cancer Therapy, Medicine
Boston Scientific's Guidezilla Guide Extension Catheter has secured 510(k) approval from the US Food and Drug Administration (FDA) and CE Mark, which would enable the company to market the device in the US and European markets. The ...
The US Food and Drug Administration (FDA) has permitted the sale of Verify Cronos Self Contained Biological Indicator (SCBI), a new quicker testing method to check the effectiveness of steam sterilization of reusable medical devices. ...
Taking an important first step toward reducing Americans' unnecessary exposure to arsenic in foods, the U.S. Food and Drug Administration is proposing an "action level" of 10 parts per billion for inorganic arsenic in apple juice, which is ...
Tags: Apple Juice, Arsenic
The U.S. Food and Drug Administration (FDA) will publish a final rule amending the food additive regulations to no longer provide for the use of bisphenol-A (BPA)-based epoxy resins as coatings in infant formula packaging because this use ...
CryoLife has received premarket approval from the US Food and Drug Administration (FDA) for its new Sologrip, a minimally invasive laser fiber-optic delivery system. The Sologrip delivery system is a single-use, disposable handset ...
DJO Global has launched its Empi Phoenix, an electrical stimulator that simplifies the treatment of muscle atrophy pre and post surgery for total knee replacement or ACL repair. The Empi Phoenix is a prescription medical device that ...
Tags: Knee Treatment, Medicine
The US Food and Drug Administration (FDA) is set to publish a final rule amending the regulations on food additives to no longer provide for the use of bisphenol A (BPA)-based epoxy resins as coatings in infant formula packaging. Based on ...
Tags: Infant Food Packaging, Packaging