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Lost in Transition Telephones
Lost in Transition

Treating rare disease shouldn’t be like a bad game of telephone, with each step generating chaos and confusion. Patient adherence suffers, quality of care diminishes, manufacturers miss out on vital feedback and cost goes up. But imagine if you could cut past all that. We did.

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DOHMEN NEWS

Learn what's happening in the world of Dohmen and our clients
May 08, 2017

Dohmen announces new Vice President, Contracting and Payer Access, DLSS

Dohmen has appointed Brian Davis as its new Vice President of Contracting and Payer Access for orphan drug manufacturers for Dohmen Life Science Services. With 15 years of experience in managed care contracting, he has held roles leading both contracting and compliance departments. He’s also a pharmacist and has an extensive background in public policy and professional regulation.
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March 27, 2017

Dohmen releases new white paper on improved outsourcing model for orphan drug manufacturers

The $114 billion orphan drug industry is traditionally served by a multi-channel model of disparate service providers. Each claims expertise in a specific niche of services, yet therapy adherence for rare disease patients is just over 58 percent. The Dohmen Life Science Services white paper explores an integrated outsourcing model that’s driving better adherence, supporting healthier outcomes and helping orphan drug manufacturers continuously improve their patient program with lower cost and less risk. Industry experts and patient advocates weigh in on why business process outsourcing must evolve.
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February 27, 2017

Dohmen unveils infographic recognizing importance of Rare Disease Day 2017

This week Dohmen Life Science Services joins millions of people in recognition of Rare Disease Day on February 28 – a worldwide effort to raise awareness for the patients and caregivers impacted by rare disease every day.
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December 20, 2016

Dohmen’s Wendy White named Global Genes Chairman of the Board

Global Genes, one of the world’s leading nonprofit rare disease patient advocacy organizations, recently named Wendy White, Dohmen Life Science Services (DLSS) Senior Vice President, Rare Disease, as the Chairman of the Board.
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November 22, 2016

Dohmen sponsors annual HBA conference helping transform women leadership in healthcare

Dohmen Life Science Services recently joined more than 900 industry leaders at the annual Healthcare Businesswomen’s Association (HBA) conference. As one of three Diamond sponsors, DLSS helped shine light on the importance of women leaders in healthcare.
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November 17, 2016

Twelve months & counting: Are you ready for DSCSA?

Upcoming Drug Supply Chain Security Act (DSCSA) legislation outlines critical steps to identify and trace certain prescription drugs as they are distributed in the United States. The new requirements impact manufacturers, repackagers, wholesalers, dispensers and third-party logistics providers to varying degrees. Pat McGinn, DLSS expert for DSCSA compliance, shares these top 5 tips for manufacturer readiness.
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October 27, 2016

Dohmen announces new Vice President, Quality Assurance Consulting, DLSS Compliance Services

Dohmen has appointed Kimberly Garko, Ph.D., MS, as Vice President of Quality Assurance (QA) Consulting, Compliance Services with Dohmen Life Science Services. Garko will develop and manage QA consulting programs for pharma, biologic and medical device manufacturers to ensure their processes are compliant with industry regulations and standards
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October 25, 2016

Dohmen’s Chief Scientific Officer shares drug development predictions at NORD annual summit

Hundreds gathered this month at NORD’s Rare Diseases and Orphan Products Breakthrough Summit in Arlington, VA. Patients and caregivers joined leaders in the FDA, NIH, industry and payer community to address critical issues in rare disease. Speakers reported on progress in diagnosis, treatment, patient engagement and market access of orphan products. Eric Floyd, PhD, MBA, Chief Science Officer and President of Compliance Services, Dohmen Life Science Services, joined leaders from the NIH and FDA in an afternoon panel, “Predicting the Pipeline – Orphan Product Development and Progress in 2017.”
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