Newsletter | January 8, 2026

01.08.26 -- Fostering A Quality Software Culture

INDUSTRY INSIGHTS

Practical Strategies For Risk Control In Document Reviews

Struggling with chaotic reviews and missed deadlines? Laura Oberthur-Johnson, Ph.D., shares practical strategies to streamline document reviews and lead with confidence and clarity.

4 Signs That It's Time For DataOps

Discover when it’s time to integrate innovative solutions into your tech stack, as well as learn how DataOps and industrial data orchestration can drive ROI and streamline manufacturing operations.

3 Reasons Why Manufacturers And CDMOs Are Integrating QA/QC

Life sciences manufacturers are integrating QA, QC, and production to boost efficiency, reduce downtime, and scale smartly. Explore how Industry 4.0 technologies are reshaping operations.

FROM THE EDITOR

Fostering A Quality Software Culture

Transforming the quality culture should include the adoption of software quality engineering (SQE), but what is it, and how can it impact the quality of your products and processes?

INDUSTRY INSIGHTS CONTINUED

Improve Scalability And Manufacturability Of A Cytotoxic ADC

Learn about the process conditions and protocols that were chosen as optimization targets and the resulting improvements to ADC production and purification that assessing these parameters provided.

Aseptic Environmental Monitoring For Vaccine Manufacturing

To meet immediate vaccine demand, aseptic manufacturing capacity must increase quickly. This means environmental monitoring programs must adapt rapidly as well. Thoughtful planning can help.

How To Capture Growth In The Expanding Metabolic Drug Market

Driven by GLP-1 success and rising obesity rates, R&D investment in metabolic disease therapies now rivals oncology, demanding rapid development to overcome market challenges.

How DFM Promotes Scalability, Repeatability, And Profitability

Find out why it is critical that OEMs see and understand the benefits of taking time to build a mold or create automation more robustly to achieve long-term savings and higher annual production.

Parenteral Manufacturing And Packaging Trends

Parenteral drug manufacturing is undergoing a rapid transformation, driven by emerging technologies and shifting market demands. There is a growing emphasis on patient-centric design and usability.

Developments In OSD Manufacturing: What Biotechs Need To Know

Oral solid dose (OSD) manufacturing advances address poor solubility and HPAPI handling through innovations like advanced formulation, enhanced containment, and flexible digitalized suites.

Advancing Topical Formulations With Innovative Preclinical Models

A robust formulation development approach integrates scientific principles and systematic formulation development to facilitate early identification of candidates with poor developability.

5 Key Questions On Implementing Pharma 4.0™ Solutions For Fill-Finish

Pharma 4.0 leverages IoT, AI, and automation to enhance drug quality. Evaluate your fill-finish line readiness by considering five key questions on modularity, process automation, and data integration.

4 Things To Consider In Pharmaceutical Labeling

Pharmaceutical labeling demands precision. Examine key considerations for ensuring accuracy and efficiency in your process, from robust control systems to diverse printing options.

SOLUTIONS

A Modern Pharma MES Solution Offers The Best Of Old And New

Protein Degraders: From Discovery To Development

An Automation Platform That Drives Data Mobility

Partner With The Experts In Annex 1

Cleaning And Disinfectant Bucket System For Manufacturing

An Organ-Chip Platform That Generates Human-Relevant Data At Scale

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