Thursday, October 16, 2014

FDA Announces Availability of Draft Guidance Regarding Licensure Standards Under Title II of the DQSA - News - National Association of Boards of Pharmacy® (NABP®)

Read the full article: FDA Announces Availability of Draft Guidance Regarding Licensure Standards Under Title II of the DQSA - News - National Association of Boards of Pharmacy® (NABP®):

"FDA is issuing this document, “The Effect of Section 585 of the FD&C Act on Drug Product Tracing and Wholesale Drug Distributor and Third-Party Logistics Provider Licensing Standards and Requirements: Questions and Answers,” (PDF) to help stakeholders understand the immediate effects of the law and to clarify section 585’s effect on state product tracing requirements, and on standards, requirements, and regulations related to licensing wholesale distributors and/or third-party logistics providers (3PLs)."

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Friday, October 3, 2014

CAMPS Co-Locates 2015 Meeting at Medtrade -- HME Business

Read the full article: CAMPS Co-Locates 2015 Meeting at Medtrade -- HME Business:

"The California Association of Medical Product Suppliers (CAMPS) will combine its annual meeting with Medtrade Spring, scheduled for March 30-April 1, 2015.

 “This co-location agreement saves CAMPS members time and money by allowing them to go to one trade show instead of two in 2015,” said Kevin Gaffney, group show director, Medtrade. “CAMPS members will have full access to the Medtrade Spring show floor and all educational sessions, and we will have the privilege of welcoming CAMPS members to what will be an excellent show at the Mandalay Bay Convention Center in Las Vegas.”"

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Thursday, October 2, 2014

Genentech's distribution change for cancer drugs upsets hospitals | Modern Healthcare

Read the full article: Genentech's distribution change for cancer drugs upsets hospitals | Modern Healthcare:

"Drugmaker Genentech is changing the way it ships three high-profile cancer drugs to hospitals, which are concerned that the new process will grossly inflate their already high costs and potentially affect patient care. Genentech contends the change is designed to ensure patient safety and access to the drugs involved.

In a Sept. 16 letter to hospital pharmacy directors (PDF), Genentech, a U.S. subsidiary of Swiss healthcare giant Roche, said effective Oct. 1, hospitals can receive Avastin, Herceptin and Rituxan only through six authorized specialty distributors. The approved companies are ASD Healthcare, BioSolutionsDirect, Cardinal Health Specialty Distribution, McKesson Plasma and Biologics, Morris & Dickson Specialty Distribution and Smith Medical Partners.

For hospitals, this means they will have to contract with one of those specialty distributors if they want to continue receiving those three cancer drugs. Previously, hospitals purchased the drugs through wholesale distributors, which offer hospitals discounts based on purchase volume."

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