The FDA cleared an investigational new drug application for a phase 2 trial of GRF312 ophthalmic solution, an immunoglobulin ...

Ophthalmology Times - ophthalmology news, articles, and events in a timely and accurate manner for members of the ophthalmic ...

The US Food and Drug Administration (FDA) has cleared Grifols' investigational new drug (IND) application to initiate a Phase ...

Patients with glaucoma or dry eye disease are likely to have additional systemic conditions that makes self-administration of drops difficult.

LUMIFY eye drops were initially introduced by Bausch + Lomb in 2018 and remain the only OTC redness relievers that ...

Nationwide recall affects five types of dry eye treatments due to manufacturing violations and sterility concerns.

Pharmaceutical company AvKare has issued a voluntary recall on several of its over-the-counter products for dry and irritated ...

More than 75,000 cases comprising more than 1.8 million cartons of consumer level dry eye drops have been voluntarily recalled.

A testing lab recalled more than 75,000 cases of eye drop solution after the FDA found deviations from proper manufacturing ...

A pharmaceutical distributor issued an urgent notice about a voluntary recall for five over-the-counter eye care products ...

Millions of cartons of eye drops and other eye products have been recalled nationwide due to manufacturing and quality issues. The company AvKARE issued the voluntary recall after issues were ...

André 3000 floats to the tune of his own key. Quite literally. A week after Outkast was announced as Rock & Roll Hall of Fame inductees, the Atlanta rapper, flutist and now pianist has yet to ...