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Rapid delivery of toxicological material

Drug Target Review

The current landscape of protein drug development is characterised by accelerated timelines where new drugs are approved in months rather than years. In our experience, reaching a rapid drug substance material delivery to support toxicology studies is becoming a major milestone on the Phase I CMC clinical development path (Figure 1).

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The golden era of GLP-1 drugs: How will it impact medicine and society?

BioPharma Drive: Drug Pricing

Its new CEO has to figure out what’s next.

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[Podcast] Trial Trailblazers: Behind clinical breakthroughs

BioPharma Drive: Drug Pricing

Most Popular Biotech funding plummets as Trump policies unnerve investors: Jefferies Bispecific cancer drugs, data caveats and funding alarms: 3 takeaways from ASCO FDA to use new review tool on Sarepta’s gene therapy work FDA meeting gives window into gene therapy field’s angst Library resources Playbook First-Void Urine Testing: A Simpler Option (..)

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FDA’s AI tool ‘Elsa’ is here, and the industry has questions

BioPharma Drive: Drug Pricing

Bloomberg 23andMe’s DNA Data Gets Boosted $305 Million Bid in New Auction View all Events 17 JUN Webinar | 10:30 a.m. Its new CEO has to figure out what’s next.

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Transforming cancer care through clinical excellence

Drug Target Review

I sequenced the complementary DNA (cDNA) encoding RAS GTPase Activating Protein, a protein known that regulates cell growth, differentiation and survival of cells; mutations in these proteins are linked to cancer. My proudest achievement is my leadership journey building legacy organisations, processes and tools in clinical operations.