Newsletter | April 25, 2025

04.25.25 -- Innovation In Life Sciences: Human Factors, AI Audits, And CDMO Insights

SPONSOR

We know how tough it can be to find the right CDMO, especially when capacity is tight and timelines are critical. That's why we're bringing together 31 CDMOs for our Outsourced Pharma Capacity Update Partners Week — a chance to explore their latest capabilities and available capacity, all from the convenience of your screen. Learn more about our sessions grouped by modality to join us to find the right partner for your project.

INDUSTRY INSIGHTS

Human Factors Testing: Engaging End-Users In Med Device Development

Explore the significance of human factors in the development of medical devices through an illustration of how important it is to incorporate the end users in the device development process.

Nitrosamine Control In Peptide APIs And Drug Products

Pharmaceutical scientists and engineers must advance robust, sensitive, and efficient nitrosamine detection and control methods to safeguard public health and regulatory compliance.

FEATURED EDITORIAL

How AI Is A Game-Changer For Auditing Compliance And Efficiency

In the life sciences, audits have long been bogged down by repetitive tasks. AI is changing the way auditors operate, making compliance more seamless than ever.

They Said What? Unexpected Insights Into CDMO Selection

An assortment of conversations with experienced biopharma executives have generated some surprising commentary about CDMO selection. Chief Editor Louis Garguilo puts those insights together, covering selection preparation/responsibilities, and some interesting CDMO behaviors of late.

INDUSTRY INSIGHTS CONTINUED

Using Synthesis And Route Design Technology To Approach API Complexity

Leveraging computer-aided synthesis design technology and route scouting in the early stages of development can aid you in designing an efficient and cost-effective path to API manufacturing.

Emerging Trends In The CDMO Landscape With Bend Bioscience

In this interview, Michael discusses how the company is adapting to emerging trends in the CDMO landscape, driving innovation, and enhancing pharmaceutical product development.

SPONSOR

Webinar: Utilizing a Stepwise Approach for Nitrosamine Risk Mitigation

Mandatory nitrosamine testing has driven stricter standards for drug development. Join Cambrex's Todd Sprouse as he shares a stepwise, product-specific approach to detect, quantify, and control nitrosamine impurities efficiently. Key topics include risk evaluation, formation feasibility, analytical method development, and mitigation through targeted testing of materials. Click here to learn more.

SOLUTIONS

Pharmaceutical Solutions

Consider the wide breadth of services offered by Grace, including product development, analytical method development, project management, and custom chemical synthesis.

Improve The Bioavailability Of Poorly Soluble Drugs

KinetiSol is a fusion-based, solvent-free process that utilizes frictional and shear energies — in a fraction of the time of other amorphous solid dispersion technologies.

CDMO Capabilities

We offer a strategic partnership that enables pharmaceutical companies to leverage specialized expertise and scalable capacities without the need for substantial internal investments.

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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