BRANY

Quintiles selects BRANY as U.S. Prime site

Monday, April 22, 2013 11:48 AM

BRANY (Biomedical Research Alliance of New York) has been designated a Quintiles Prime Site. The designation will advance BRANY’s participation in clinical trials by providing improved access to new industry-sponsored clinical trials.

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BRANY to collaborate with U of Miami

Wednesday, May 23, 2012 01:50 PM

BRANY (Biomedical Research Alliance of New York) has agreed to provide education content for the Collaborative Institutional Training Initiative (CITI) at the University of Miami for use on their online clinical research training program.

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BRANY, Veritas IRB to provide AAHRPP-accredited services in U.S. and Canada

Friday, May 11, 2012 12:38 PM

BRANY (Biomedical Research Alliance of New York) and Montreal-based Veritas IRB have partnered to provide clinical trial review, compliance and other IRB services in both the United States and Canada.

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BRANY appoints Brower accounting manager

Saturday, January 21, 2012 08:56 AM

BRANY, Biomedical Research Alliance of New York, has hired Donna Brower as accounting manager to oversee the accounts payable and billing and collections departments.

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BRANY licenses SMART system to Tech Software

Wednesday, August 31, 2011 12:56 PM

BRANY (Biomedical Research Alliance of New York) has licensed its proprietary SMART (Study Management and Revenue Tracking) system to Tech Software, an information technology company that currently offers IRBManager, a fully Web-based software product that supports the administration of institutional review boards at leading hospitals throughout the country.

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Two added to BRANY team

Wednesday, April 27, 2011 12:06 PM

Biomedical Research Alliance of New York (BRANY) has added two industry experts to their team to support clinical trial sites. 

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Lack of recruitment, missed patient visits among new researchers’ common mistakes

Monday, November 22, 2010 09:01 AM

Some private-practice physicians who decide to conduct clinical trials can have trouble meeting enrollment goals because they forget to speak with their patients about study participation. Others inadvertently miss a patient visit and have to fill out numerous forms explaining why they deviated from the clinical trial protocol. 

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