Newsletter | October 2, 2025

10.02.25 -- Reliably Predicting Biologics Hotspots From Prior Knowledge

SPONSOR

Webinar: Enabling Continuous Process Intelligence: In-Line PAT Solutions for cGMP Environments

Boost efficiency and compliance in bioprocessing with Repligen’s upcoming webinar on process analytical technology (PAT). Explore real-world applications of the FlowVPX® and MAVERICK® systems for real-time monitoring of critical parameters, smarter decision-making, and reduced costs. See how PAT streamlines upstream and downstream workflows, accelerates production, and supports GMP compliance—all while cutting deviations and saving valuable time. Click here to learn more.

FOCUS ON MANUFACTURING CONTROLS

Reliably Predicting Biologics Hotspots From Prior Knowledge

Site-specific post translational modifications can seriously affect a molecules stability, function, and structure. These modifications are commonly called "hotspots."

Industry 4.0 Project Stuck In Pilot? Address These 5 Challenges

Industry 4.0 is gaining momentum, but scaling remains a challenge. Discover why a robust industrial data strategy is essential and the top five barriers keeping manufacturers stuck in pilot purgatory.

How Automated Analytical Devices Are Driving Smarter Biomanufacturing

Precision is critical in biomanufacturing. Learn how automated analytical devices are providing real-time, high-resolution data for smarter decision-making and enhanced process control.

Mastering Asset Management In CGT

Explore how CGT manufacturers can boost compliance, scalability, and efficiency by adopting purpose-built EAM/CMMS platforms tailored to their unique operational and regulatory needs.

Solving Data Challenges In Life Sciences Across The Enterprise

Unlock smarter pharmaceutical data management with an innovative platform to streamline compliance, accelerate tech transfer, and harness real-time insights to drive innovation.

Why Established Pharma Sites Need A Digital Cleaning Validation Strategy

Pharmaceutical facilities face mounting pressure to modernize. Uncover how digital tools are transforming cleaning validation to boost compliance and audit readiness without disruption.

T-Cell Manufacturing: When Is The Right Time To Automate?

Automation enhances efficiency and minimizes contamination risks and labor costs. Despite the initial investment in automation equipment, the long-term savings can be significant.

MANUFACTURING CONTROLS SOLUTIONS

A Cloud-Based Quality And Compliance Solution - Honeywell Life Sciences

Real-Time Data Management, Visualization, And Analysis - Koerber Pharma

SPONSOR

Overcoming Downstream Challenges in Next-Generation Antibody Development

How do you overcome the significant downstream purification and process challenges associated with turning next-generation antibodies into scalable, GMP-ready therapeutics? Implement a “design with the end in mind” approach, embedding commercial readiness into process development from the earliest stages. Join us October 8th at 11am ET/4pm BST to learn how. Click here to register.

FOCUS ON FACILITIES DESIGN

The Case For Pre-Owned Equipment In Drug Manufacturing

Discover how used equipment can deliver faster ROI by eliminating long lead times and reducing capital outlay, allowing for quicker production and revenue generation.

Prioritize Cleaning & Disinfection During Facilities Design

Thorough consideration of cleaning/disinfection during facility design eases maintenance across the facility lifecycle, optimizes workspace utility, and contributes to efficient facility operation.

FACILITIES DESIGN SOLUTIONS

Cleaning Detergent: Low-Foaming High Alkaline Liquid - Alconox Inc.

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