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511 Davis Drive, Suite 100, Morrisville, NC, 27560, US
When initiating a development program for drug delivery to the lungs, selection of the dosage form warrants careful consideration.
Released By Kemwell Biopharma
Dr. Barker is an experienced clinical immunologist with broad executive experience across both big pharma and biotech.
By: Charlie Sternberg
CEO Owen Murray on driving innovation with high science and high service.
By: Tim Wright
Industry experts weigh in on current trends, challenges, and the future of the cell and gene therapy CDMO market.
The CDMO's head of development talks about ADCs, accelerated timelines, and the push for end-to-end development services.
Symbiosis recorded zero GMP observations from the FDA during the inspection in January 2025.
Transitional outsourcing models, combined with a broken site feasibility process, could open opportunities for CROs to differentiate.
By: Christine Senn, PhD
Massive overhaul in works to embed greener processes.
By: Soman Harachand
Engagement is the key to addressing Scope 3.
By: Davuluri Sucheth Rao
Dr. Lutz Hilbrich brings over 20 years of experience in the biotechnology and pharmaceutical sectors.
Strategies to ensure accessibility and affordability of innovations globally.
Where big pharma stands in the face of nimble tech-driven start-ups, the impact of layoffs, and what we can expect from M&A in the future.
By: Kristin Brooks
Collaboration leverages Kemwell's manufacturing excellence and RevOpsis' Rev-Mod platform to expedite the development of novel multispecific biologics.
Singota Solutions’ Senior Director of Business Development offers his thought leadership.
By: Contract Pharma
Introduces two novel platform services for developability assessment and pre-formulation screening for ADC candidates.
The chief executive of Botanical Solution Inc. (BSI) speaks about the development of QS-21 adjuvant for vaccines from Quillaja saponaria trees grown in BSI labs
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