Newsletter | April 21, 2026

04.21.26 -- Where Contamination Control Really Breaks Down In Practice

SPONSOR

Regulatory Expectations for continued Process Verification Featuring Regulatory Expert Peter Baker (Live Oak QA)

Join this webinar to gain practical insights into regulatory expectations for CPV and strengthen your approach to maintaining process performance throughout the product lifecycle.

INDUSTRY INSIGHTS

Identify And Mitigate Absorption Risks With PBPK Modeling

See how PBPK models combined with custom and off-the-shelf in vitro tools and solubility enhancement expertise can reduce the need for drug product reformulation or repeated preclinical or clinical studies.

A New Look At Subcutaneous mAb Delivery Using Nanoformed Particles

A highly concentrated non-aqueous suspension of an IgG1 was developed using a patented platform. Review how the particle size of the mAb impacts the overall behavior of the drug product.

Sustainability Through Automation, Flow Chemistry, And Biocataysis

Learn how modeling, high-throughput tools, and advanced analytics enable safer, more efficient routes and support scalable solutions for complex chemical and enzymatic processes.

FEATURED EDITORIAL

Where Contamination Control Really Breaks Down In Practice

Contamination control gaps arise when two dynamics merge — when processes become familiar and workloads increase. Here's how to spot them before they spin out of control.

INDUSTRY INSIGHTS CONTINUED

Development Of Scalable Purification For Biotherapeutic Peptides

Discover key strategies for reversed-phase isolation of biotherapeutic peptides, as well as method development, scale-up techniques, and RP/MS analysis to enhance purification workflows.

Optimizing CMO Partnerships

Gain expert insight into best practices and tips across a range of topics, including program management, automation, and secondary services.

Metal Detectors And X-Ray Inspection Systems: What You Need To Know

Uncover how to kick the product inspection challenges of product and package effects to detect foreign objects and contaminants, keep consumers safe, and protect your brand image.

AI And Digital Maturity In Contract Development And Manufacturing

Explore how CDMOs are navigating digital maturity, where AI is driving real operational gains, and why sponsor expectations are accelerating the push toward digital readiness.

Automated Precision Powder Filling For Annex 1

Aseptic powder filling is complex, demanding automation and isolator‑based, weight‑controlled dosing to ensure sterility and accuracy.

Accelerating Antibody-Drug Conjugate (ADC) Development

Find out how automated immunoassays help overcome ADC bioanalysis challenges, reducing hands-on time, improving throughput, and enabling multi-analyte workflows for more efficient assessments.

Facilitate Handling Of Bulk Powders With Dry Granulation

Handling bulk powders in manufacturing presents serious challenges—from unpredictable caking to safety risks—that can disrupt workflows. Reveal solutions to streamline operations.

Barrel Filling Vs. Tip Filling A Syringe – Which Approach Should Be Used?

There are two primary filling methods for pre-filled syringes. Observe the pros and cons of each approach, highlighting why barrel filling is generally preferred in the pharmaceutical industry.

Inside The Cleanroom: Training Beyond The Checkbox

Effective cleanroom management requires moving beyond checkbox compliance. Watch how to empower your workforce by connecting individual roles to broader contamination control goals.

The Case For A Facility Monitoring System

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

Overcome Common Pre-Filled Syringe Challenges Through Partnership

The pre-filled syringe space is one of the fastest growing pharma sectors, offering greater patient safety and lower manufacturing costs. But pre-filled doesn’t translate to easily filled.

SPONSOR

How Connected Manufacturing Operations Unlock AI's Potential to Optimize Production

MasterControl’s latest research reveals a clear truth: AI can’t deliver without connected systems first. In this webinar, discover how siloed ERP, MES, QMS, and LIMS platforms drive delays, rework, and compliance risk, and why integration is the missing link. Learn practical steps to build a connected data foundation that improves batch release, boosts visibility, and prepares operations for AI. Click here to learn more.

SOLUTIONS

Custom Solution Partner: Specialized Capabilities, Expert Execution

The Organ-Chip Portfolio

Original Equipment Manufacturer

Efficient Process Lifecycle Management For Drug Development

Biologics: Development And Drug Substance Manufacturing

Bring Advanced ASD Tech Into Your Lab

Transform GMP Data Into Actionable Intelligence

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