Newsletter | March 7, 2025

03.07.25 -- 9 Reasons Why You Should Consider AI In Analytical Instrument Qualification

FEATURED EDITORIAL

9 Reasons Why You Should Consider AI In Analytical Instrument Qualification

AI is about to completely change the analytical instrument qualification (AIQ) landscape in the pharma/biopharma and medical device industries.

Fabled Route-Scouters Riding AI Applications

Route scouting professionals – self-effacing hunters of small-molecule simplicity, searching for efficient pathways to commercial success, fearless in pointing out risks, and at times, dead ends. Today they face mounting challenges. Can artificial intelligence (AI) bring more clairvoyance to these battered scientists? “Absolutely,” says Dr. Jürgen Swienty-Busch of Elsevier.

INDUSTRY INSIGHTS

Simultaneous Spray Drying For Combination Dry Powder Inhaler Formulations

Three combination case studies are demonstrated, in which bevacizumab is paired with erlotinib, cisplatin, or paclitaxel in a dry powder inhaler formulation.

Nose To Brain (N2B) Drug Delivery – Benefits And Challenges

Delve into the growing interest in drug delivery methods that target the brain and central nervous system via absorption into the bloodstream, specifically focusing on crossing the blood-brain barrier (BBB).

Outsourcing High Potent Oral Solid Dose Late-Stage Development: CDMO Insights

This presentation discusses outsourcing options for highly potent oral solid dose therapies and explains how CDMOs can transfer, handle, and deliver their product to clinics and to market.

Leveraging CDMOs In Pharma's Drive Toward Net Zero

Environmental considerations in pharmaceutical manufacturing strategies have become increasingly important in the face of additional calls to address pollution and sustainability practices globally.

Asset Reinduction To Maximo EAM, Enabled By Reality Capture

Find out how reality capture was used to create a digital twin 750,000-square-foot Pfizer campus to support asset reinduction to Maximo EAM, saving Pfizer 3,000 hours per year.

SOLUTIONS

A Technology-Driven CDMO Delivering Integrated End-To-End Services

Explore this interactive PDF with information about technologies and end-to-end integrated CDMO services, encompassing taste masking, controlled release, solubility enhancement, and dosing solutions.

Innovation In Medicinal Chemistry – India’s Expertise

Consider our global network’s cutting-edge medicinal chemistry capabilities and streamline your outsourcing needs with cost-effective solutions.

Advancing Small Molecule Development

Partner with Curia’s global team of experts to streamline process development, scale-up, and cGMP manufacturing for your small molecule projects.

OUTSOURCED PHARMA CAPACITY UPDATE

Find Your New CDMO At Outsourced Pharma Capacity Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capacities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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