Newsletter | April 12, 2024

04.12.24 -- Fine-Tuning Analytical Development Strategies For Every Phase

FEATURED EDITORIAL

Fine-Tuning Analytical Development Strategies For Every Phase

Analytical challenges morph phase-by-phase during drug development. Here, three Novartis scientists describe a platform approach based on guidance from the ICH and USP.

INDUSTRY INSIGHTS

Understanding The Importance Of Powder And Vapor Containment

Have you considered the safety of your work environment’s air? Across industries, employers are determining how to detect inhalation hazards and, if present, how to protect employees from them.

How The Quality Culture Impacts GMP Activity

Londa Ritchey shares invaluable insights derived from her extensive experience, shedding light on the pivotal role of fostering a strong quality culture in maintaining GMP compliance.

Reasons Blow/Fill/Seal Technology Should Be Considered For Aseptic Filling

Drug manufacturers seeking alternative methods for a safe and reliable approach to drug delivery should consider blow-fill-seal technology, as it offers several benefits over traditional glass packaging.

Microplate Readers In Cancer Research

Understanding the basics of microplate readers and their applications allows researchers to make significant strides in understanding and ultimately conquering cancer.

The Potential Of Networked LC-MS Systems In Analytical Laboratories

Learn how networked Liquid Chromatography-Mass Spectrometry (LC-MS) systems can address the challenges in analytical laboratories, enabling the optimization of data generation and overall efficiency.

Automated Data Integrity In Sterility Testing

Explore trends and challenges in microbiology QC with Anne Weeks, a senior field marketing manager at MilliporeSigma. She discusses workflow automation and introduces a customizable MTR solution.

Container Closure Integrity Testing: Risks And Methods

We share an overview of integrity tests where high sensitivity is required to prevent the risks of stability failure of highly moisture-sensitive drugs or biological ingress of sterile parenteral drugs.

Making The Case For Case Management For Cell And Gene Therapies

It is crucial to ensure that CGT supply chain risks are mitigated, as well as to have proactive strategies in place to address unforeseen challenges before they become an issue.

Successfully Producing Insoluble Proteins Using Inclusion Bodies

Review the pros and cons of soluble and insoluble processes, experiences with isolating, solubilizing, and properly re-folding, and strategies and innovation to improve insoluble processes.

Increasing Delivery System Flexibility Through Solvent-Based Processing

Learn how a biodegradable polymer platform that is compatible with many substrates can enable several applications as a drug eluting carrier with a wide variety of APIs.

Intro to USP <1062> — What Is Tabletability?

What is tabletability, and why is it important for creating tablets that can survive the journey from manufacturing to packaging?

Introducing Robust, Easier-To-Use Detergent Packaging

Gain insight into the most recent upgrades to Alconox's powder detergent packaging and the company's focus on continuous improvement from the Vice President of Strategy, Michael Moussourakis.

Why KinetiSol Is Disrupting Spray Drying

Review a commercially ready process capable of reproducing spray-dried dispersions with less manufacturing complexity and environmental impact that can out-design and outperform spray drying.

SOLUTIONS

An Introduction To Isolated Robotic Aseptic Filling Systems

Small Molecule Capacity Update

Pharmaceutical Mixers For Sterile/Aseptic Manufacturing

Bulk API Contract Manufacturing

Downstream Digital Twins. Biopharma Going In Silico

Pharmaceutical Clinical Trial Distribution Services

Sampling And Dispensing Services

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