PHARMACY

ScriptPro wins top spot in KLAS rankings

BY Alaric DeArment

MISSION, Kan. — Pharmacy automation system manufacturer ScriptPro has received a top spot from a research firm that specializes in monitoring and reporting on the performance of healthcare vendors.

ScriptPro said the healthcare IT research firm KLAS ranked its SP Central Pharamcy Management System No. 1 in the category of Software Solutions – Pharmacy – Outpatient (Retail) in the "2012 Best in KLAS Award: Software & Services."

"We really value the KLAS ratings. They give us objective information on how we’re doing from the perspective of our customers," ScriptPro president and CEO Mike Coughlin said. "They also help focus the attention of our team on the all-important mission of continuously improving and providing products and services that we can all be proud of."


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PHARMACY

Actavis can launch generic painkiller in May 2014 under settlement

BY Alaric DeArment

PARSIPPANY, N.J. — Actavis and Mallinckrodt have reached a settlement concerning the former’s generic version of an opioid painkiller made by the latter, Actavis said Thursday.

The companies settled patent lawsuit regarding Actavis’ generic version of Mallinckrodt’s Exalgo (hydromorphone hydrochloride) extended-release tablets in the 32-mg strength. The companies settled litigation regarding the 8-mg, 12-mg and 16-mg strengths last month.

Under the settlement, Mallinckrodt granted Actavis a loyalty-free license to its U.S. patents on Exalgo, allowing Actavis to start selling the 32-mg strength in generic form starting in May 2014. Actavis said it was likely the first company to file for Food and Drug Administration approval of a generic version of the drug, which would entitle it to 180 days in which to compete exclusively against the branded version after approval.


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PHARMACY

Eisai receives orphan drug designation for thyroid cancer drug

BY Alaric DeArment

WOODCLIFF LAKE, N.J. — The Food and Drug Administration has granted special designation to a drug made by Eisai for treating thyroid cancer.

The drug maker said Thursday that its experimental drug E7080 (lenvatinib) had received orphan drug designation from the FDA for follicular, medullary, anapestic and metastatic or locally advanced papillary thyroid cancer.

The FDA grants the designation under the Orphan Drug Act for products that treat, diagnose or prevent a rare disease or disorder affecting fewer than 200,000 people in the United States. Orphan drug designation entitles a company to tax credits, extended market exclusivity following regulatory approval and other benefits.


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