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Rethinking antibody discovery in the age of automation

Drug Target Review

This focus has allowed the company to serve not only large-scale industry users, but also academic groups and researchers in emerging markets who may otherwise lack access to advanced automation. James obtained his PhD in Analytical Chemistry from the University of Georgia. Still, barriers remain – particularly for smaller labs.

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Calibre Scientific Expands European Presence and Chromatography Offering With AIT France Acquisition

The Pharma Data

25, 2021 (GLOBE NEWSWIRE) β€” Calibre Scientific is pleased to announce the acquisition of AIT France (β€œAIT”), a manufacturer and distributor of innovative consumables for analytical chemistry and chromatography. LOS ANGELES, Jan. Our global reach extends into over 100 countries, empowering customers all over the world.

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Embarking on a Career in Drug Development

Alta Sciences

A: Drug development uses a lot of the same skills as forensic scienceβ€”the analytical chemistry, the problem-solvingβ€”with just a different application. Every time I learn of one of the drugs we’ve worked has moved into clinical trials or has gone to market, I'm further motivated. Q: What drew you to drug development?

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Beyond the Lab: Commercial Careers in Life Science

Elrig

We invited a panel of speakers to share their experience & insights, watch the video below to hear their insights: How do you recommend marketing your CV for moving over into a more commercial role? I have a year long masters project based within a CRO’s analytical chemistry innovations department initially working in the lab.

Science 40
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WhyIScience Q&A: How a chemist moved to the business side of science

Broad Institute

WhyIScience Q&A: How a chemist moved to the business side of science By Corie Lok April 16, 2025 Breadcrumb Home WhyIScience Q&A: How a chemist moved to the business side of science Diane Diehl talks about how she has gained marketing, business development, and operations skills while leading scientific teams throughout her career.

Science 69
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New Draft Guidance Provides Detailed (and Burdensome) Recommendations for Chemical Assessments to Support Medical Device Biocompatibility

FDA Law Blog: Biosimilars

FDA also notes variability in the approaches, inconsistent analytical chemistry reports, and deficiencies in review of premarket submissions as a driver for the draft guidance. BEP/BER or Biological Risk Assessment) per ISO 10993-1 is not required for the majority of FDA pre-market submissions.