Newsletter | December 12, 2025

12.12.25 -- Global Implications Of Zero Tariffs On Indian Pharma Exports To China

SPONSOR

Take a brief tour of Nanoform's advanced nanoformulation, nanoanalytical, and best-in-class capabilities. This video highlights Nanoform’s advanced characterization tools, state-of-the-art formulation technologies, and expert-driven solutions designed to tackle bioavailability challenges. Watch the video now.

INDUSTRY INSIGHTS

A Pragmatic Approach To Developing A Rare Disease Drug

With the rise in interest in developing "orphan drugs," or pharmaceutical agents intended to treat rare diseases, we're examining challenges and considerations associated with their expedited development.

4 Reasons For The Rise In Blister Packaging

As blister packaging is forecast to grow as a dominant packaging sector. Pharma and consumer healthcare companies hoping to expand should review their current packaging methods.

Harnessing Digital Twins To Optimize Tablet Manufacturing

Unlock manufacturing precision with digital twins. Learn how virtual replicas of production systems enable predictive maintenance, streamline scale-up, and ensure consistent product quality in pharma.

FEATURED EDITORIAL

Buckle Up. It's A Strategic Drive To Successful Sourcing

We bounce around the word “strategic” like a biopharma basketball. We’ve even got our own league. More professionals in the outsourcing industry include “strategic” in their titles than ever before. Find what this exulted approach to working with external partners really means.

Global Implications Of Zero Tariffs On Indian Pharma Exports To China

Opposing U.S. and China drug tariff policies are poised to reshape global pharmaceutical flows. Explore what these shifts mean for your market and supply strategy.

INDUSTRY INSIGHTS CONTINUED

Multifactorial Disease Models: De-Risking Topical Formulation Development

Traditional drug models fail to predict performance in human skin. Advanced, multifactorial ex vivo disease models directly address inflammation and infection to de-risk formulation development.

Rapid Development Of A Liquid-Filled Capsule Formulation Of CBD

Discover how we developed and tested multiple oral formulations in just three months, identifying a top candidate that outperformed existing standards in key performance metrics.

Innovative Technology For Developing, Scaling Peptide-Based Therapeutics

Watch as experts walk through several technologies and case studies, focusing on liquid-phase peptide synthesis, crystallization, method development for impurity analysis, and more.

Solving Delivery Challenges For Tolerogenic Vaccines

Explore the advantages offered by an orally dissolving tablet platform relating to large molecule storage, aggregation, and, in some cases, protease activity.

Environmental Sustainability: Wastewater Incineration Reduction

This approach to wastewater treatment reduces the environmental impact of small molecule production and introduces advanced treatment methodologies to avoid wastewater incineration.

Current Strategies For Enhancing Bioavailability

Consider the following strategies for enhancing the bioavailability of poorly soluble drug compounds, including spray drying, particle size reduction, and lipid-based formulations.

SOLUTIONS

The Next Generation Of Oral Targeted Therapies

Solve the unique challenges of poorly soluble molecules like targeted protein degraders (TPDs), such as PROTACs and molecular glues, to seamlessly accelerate your molecule to commercialization.

Pharmaceutical Development

Using our knowledge of nanomaterials science and specialized nanoformation, we can help you deliver a formulation that meets your needs for oral, inhaled, injectable, and ophthalmics.

Capabilities Update July 2025: Fill/Finish

Gain an overview of a new state-of-the-art Groninger filling line’s capabilities, production scale-up timelines, and how this new infrastructure supports product flexibility and long-term growth.

South Haven cGMP Manufacturing Services And APIs

Our chemical manufacturing facilities are equipped to support a wide range of projects with on-site pilot plants and large-scale commercial capabilities for manufacturing high-quality APIs.

OUTSOURCED PHARMA CAPABILITIES UPDATE

Find Your New CDMO At Outsourced Pharma Capabilities Update

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

Connect With Outsourced Pharma: