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Integrating Excipient Innovation in Drug Development

By: Marina Ruleva
4/6/21 10:15 AM

As we prepare for future-readiness by facing the challenges related to the topic of new excipient selection, we explore the barriers to innovation.

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4 Steps to Complete Drug Manufacturing

By: Tim Brown
9/21/20 10:45 AM

Large drug companies are increasingly using contract partners strategically to fill capacity and expertise gaps to produce their branded drugs.

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Why and How to Partner with a Full-Service CDMO on Your Next Drug

By: Tim Brown
8/28/20 10:49 AM

CDMOs provide a single source for the development and manufacturing of pharmaceuticals, and they offer complete services to bring a drug to market.

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Quality Assurance Process with William Pfeiffer

By: Beau Garrett
8/3/20 7:33 AM

As the Sr Director of Quality Assurance, William joined Tapemark in March 2019, bringing over 20 years of cGMP in pharmaceutical and biopharmaceutical.

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Expert Development Processes with Tim Brown

By: Beau Garrett
7/27/20 4:12 PM

Tim has seen Tapemark evolve from a drug manufacturer to a full-service CDMO. And today, he will explain Tapemark’s Development Process.

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Expert Formulation Development + R&D with Marina

By: Beau Garrett
6/25/20 7:45 AM

Marina is responsible for ensuring client objectives, researching and developing new products and technologies, as well as improving existing products.

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Tapemark Manufacturing Facility Completes Successful FDA Pre-Approval and General GMP Inspection

By: William Pfeiffer
6/1/17 5:10 PM

The FDA has completed a successful pre-approval inspection (PAI) of Tapemark’s manufacturing process and a general good manufacturing practices (GMP) inspection.

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