Newsletter | May 20, 2025

05.20.25 -- From Preparation To Compliance: DSCSA Implementation Takes Big Steps In 2025

INDUSTRY INSIGHTS

Key Requirements To Ensure Patient Safety In Viral Vaccine Production

Gain insight into the issues and obstacles faced by pharmaceutical companies, the current regulatory framework surrounding viral vaccines, and how one company is preparing for the next outbreak.

Spray Drying To Enable New Inhaled Drug Products

The formulation and spray drying process can help manufacture a stable, highly respirable powder and deliver products that require a high drug load, a biologic, or rapid onset therapeutic.

Viral Disinfectant Efficacy Studies: Key Guiding Factors And Design Elements

Viral Disinfectant Efficacy Studies validate cleaning protocols in pharma facilities, ensuring regulatory compliance, reducing contamination risk, and supporting safe disinfection with expert CRO guidance.

Blending And Simulation: A Beginner's Guide

This beginner-friendly webinar reveals essential steps to understand mixing, reduce segregation, enhance efficiency, and improve product quality with granular materials.

The Case For A Facility Monitoring System

Facility monitoring software with OPC UA client/server functionality makes great business sense. Learn how monitoring leads to reduced waste, improved yield, higher quality, and increased profits.

Improving Bioavailability, Drug Loads, And Pill Burdens Of Solid Dispersions

Explore the pros and cons of marketed amorphous solid dispersions with so-far unpublished data as well as a green alternative to ASDs: best-in-class nanotechnology to manufacture nanocrystals.

Nasal Inhalation Delivery – An Introduction Guide

Unlock the potential of nasal inhalation for delivering active pharmaceutical ingredients by examining the benefits of both liquid and dry powder formulations as companies drive innovation in the field.

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Discover the importance of compressed gas monitoring in ensuring product quality and compliance with EU GMP standards.

Enhance Your Downstream T-Cell Processing

T-cell therapies, including CAR-T and TCR, revolutionize cancer treatment by harnessing the immune system. Uncover an efficient and scalable production process that helps meet crucial demand.

Minimizing Risk In RNA-LNP Encapsulation And Drug Product Manufacturing

Watch to learn about an integrated drug substance/drug product offering for your IND program and beyond, with a holistic approach to ensure process robustness at every stage.

A High-Throughput Platform For Fast And Reliable Clone Screening

This innovative platform consists of several technologies allowing for the cultivation and monitoring of CHO cells in cell line development. Find out how to set up your experiment on this device.

Prevention Of Product Recalls

Implement inspection systems like X-ray, vision inspection, and metal detection to help prevent contamination and regulatory issues, which ensures high product quality.

FEATURED EDITORIAL

From Preparation To Compliance: DSCSA Implementation Takes Big Steps

The phased exemption periods of the Drug Supply Chain Security Act (DSCSA) expire on different dates throughout 2025 (including one quickly approaching in May), marking a series of milestones for implementation.

SOLUTIONS

Glass Prefillable Syringe Solution Delivering Complex Biologics

Factors Which Impact mAb Process Scale-Up

End-To-End Pharmaceutical Solutions With A Softgel Specialty

Aseptic Filling Of Respiratory Therapy Bottles Using Blow-Fill-Seal

Cleaning Coveralls And Other Potentially Contaminated PPE

Connect With Pharmaceutical Online: