Newsletter | August 27, 2025

08.27.25 -- Lilly's Kinsale Facility Provides A Benchmark For Your CDMO Selection

SPONSOR

Webinar: Strategic Approaches to Controlled Release Formulation: Polymer Screening and Case Study Insights

Join Bend Bioscience for an insightful webinar on controlled release (CR) formulations—designed to optimize drug performance, enhance patient compliance, and reduce dosing frequency. Learn how to streamline CR development using efficient polymer screening methods and real-world case studies. Don’t miss this opportunity to gain actionable strategies and elevate your formulation expertise. Register now! Click here to learn more.

INDUSTRY INSIGHTS

Painkiller and Sedative Demands: Effects On Bupivacaine HCI Supply

As global authorities work to fill gaps, drug manufacturers and CDMOs have become critical in the efforts to stabilize the supply of Bupivacaine HCl and other essential drugs.

5 Dangers Of An Insecure API Supply Chain

See how diversifying API supply chain beyond multiple suppliers through geographic spread and raw material origins can promote uninterrupted medicine supply and patient access.

FEATURED EDITORIAL

Minimizing The Impact Of Human Errors Using Relational Risk Analysis

Learn how a mechanism-based risk analysis approach can provide two complementary opportunities for minimizing the likelihood of a human error impacting pharmaceutical and medical device risks.

Lilly's Kinsale Facility Provides A Benchmark For Your CDMO Selection

Consider these two questions: How do we select a CDMO? How do we select a facility? The second of these should carry as much weight as the first, but unfortunately often does not. Chief Editor Louis Garguilo thinks that should change. He turns to Eli Lilly's ISPE Award Winning facility, and Lorraine O'Shea, Associate Vice President and Plant Manager at Lilly Kinsale, to make the case.

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.

Central Nervous System (CNS) Drug Development, Simplified

Discover a global CNS leader with 200+ studies completed to date and end-to-end drug development expertise—bridging translational gaps and accelerating your path from discovery to delivery.

The Role Of CDMOs In Supporting Generic Drug Development

Bringing complex generics to market requires deep expertise. Learn how a CDMO can help navigate regulatory, technical, and commercial challenges with end-to-end development and manufacturing support.

SPONSOR

Join Outsourced Pharma Online on September 3rd at 2pm ET for a virtual panel discussion on overcoming difficulties outsourcing development and manufacturing, how does a biopharma organization (of any size) handle a multi-CDMO coordination. Registration is free for this digital event.

SOLUTIONS

Regulatory Starting Materials (RSMs) — India

The Pharma Expanse network currently spans across 9 manufacturing sites in 5 countries and can support discovery, preclinical, clinical and commercial programs for New Chemical Entities (NCEs).

Pharmaceutical Solutions

Explore a wide breadth of services, including product development, analytical method development, project management, and custom chemical synthesis.

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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