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Scientific workflow for hypothesis testing in drug discovery: Part 2 of 3

Drug Target Review

In 2003, he was selected by EE Times as one of the top 13 most influential people in the semiconductor industry. Nina Truter Nina Truter is a translational scientist with a deep focus on understanding mechanisms of action in drug development and leveraging disparate datasets in biotech.

Drugs 69
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Scientific workflow for hypothesis testing in drug discovery: Part 1

Drug Target Review

In 2003, he was selected by EE Times as one of the top 13 most influential people in the semiconductor industry. For more: [link] ; [link] ; [link] ; [link] Nina Truter Nina Truter is a translational scientist with a deep focus on understanding mechanisms of action in drug development and leveraging disparate datasets in biotech.

RNA 52
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Bridging science and technology: a biotech CEO’s perspective

Drug Target Review

Wilkie’s background as a biochemist and his time at Merck, a leading pharmaceutical company, shaped his early understanding of drug development and business strategy. As someone who describes himself as an “enthusiastic sceptic,” Wilkie is cautious but hopeful about the potential of AI in drug development. “I

Science 52
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New understanding of the TMEJ pathway in cancer

Drug Target Review

She continued: “Now that we know more about this pathway, scientists could, in theory, produce a drug that could disrupt key pieces of the pathway in cancer cells, as opposed to using conventional chemotherapies that destroy healthy cells along with the cancer.” Polymerase theta TMEJ has been the most elusive DNA repair pathway.

DNA 59
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Zigs & Zags – The Opposite of a Great Idea Can Also be a Great Idea

Perficient: Drug Development

I worked on many projects with them in my early career (2003-2013). A Real-World Personal Example – Zagging to Success A successful “zag” with a great idea doesn’t need to be risky. Atlas Van Lines is in the moving and relocation industry. We did amazing work together.

Marketing 116
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CMC Content for Global Clinical Development of Pharmaceuticals

The Premier Consulting Blog

Similarly, clinical submissions to the Central Drugs Standard Control Organisation (CDSCDO) in India accept the EU Q-IMPD format. The Dossier de Desenvolvimento Clínico de Medicamento (DDCM), translated Clinical Drug Development Dossier, is submitted to the Brazilian regulatory authority Agência Nacional de Vigilância Sanitária (ANVISA).

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Perficient Expands Executive Leadership Team

Perficient: Drug Development

Bill has led marketing at Perficient since 2003, in a period of intense growth. Bill Davis Senior Vice President, Marketing & Alliances As senior vice president of marketing and alliances, Bill Davis is responsible for Perficient’s global marketing and communications functions.