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April 19, 2016  •  News

Biologics Consulting Expands Services, Launches Clinical Trials Planning and Oversight Group

Biologics Consulting, a full-service regulatory and product development consulting firm for biologics, pharmaceuticals and medical devices, announces the launch of its Clinical Trials Planning and Oversight Group. The group will help small and medium-sized biopharmaceutical companies in the development…

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February 3, 2016  •  Webinar

Clinical and Regulatory Considerations for Orphan Drug Applications

Overview The development of Orphan Drugs - those developed specifically to treat rare medical conditions - is growing at an astounding rate. In 2014, nearly 41%1 of all new product approvals from the FDA were for the treatment of rare diseases - a trend that is expected to continue as the exclusivity…

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January 19, 2016  •  News

Biologics Consulting Unveils New Brand Identity; Launches Expert Edge Webinar Series Providing Participants Access to Top Consultants

Biologics Consulting, a full-service regulatory and product development consulting firm for biologics, pharmaceuticals and medical devices, has launched a rebranding effort that includes the introduction of new brand positioning, as well as a new logo and interactive website. In conjunction with the…

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December 22, 2015  •  Webinar

The Value of Analytics for Achieving Successful Manufacturing Process Transfer

Overview The biopharmaceutical product development lifecycle often requires the transfer of a manufacturing process from one facility to another. These transfers can occur at any point along the development path, and may be driven by increases in material needs to support clinical studies or the commercial…

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