Newsletter | November 13, 2026

11.13.26 -- Sustainability In Manufacturing: Power And Digital Twins

SPONSOR

Webinar: Mitigating risk across the OSD lifecycle: How expert CDMO partnership can build early foundations for long-term success

Early development decisions can make or break an oral solid dosage (OSD) program. Join experts from Bora Pharmaceuticals and Corealis Pharma to explore how risk management, Quality by Design, and CDMO partnerships improve scalability, streamline technology transfer, and protect product quality. Learn how to identify challenges early and support commercialization. Click here to learn more.

INDUSTRY INSIGHTS

A Unified Model for Development-To-Manufacturing Continuity

Discover how integrated digital systems can improve traceability, inventory control, compliance, and knowledge management by connecting experimental data, materials, equipment, and sample histories.

Targeted Modalities Set Elevated Standards For Precision

Explore how targeted modalities like ADCs and TPDs are transforming precision medicine, unlocking new treatment opportunities, and overcoming development challenges to improve patient outcomes.

De-Risking Production Of Complex Oral Solid Dosages

Reduce formulation and scale-up risk with integrated development and manufacturing expertise for complex OSD products.

FEATURED EDITORIAL

Sustainability In Manufacturing: Power And Digital Twins

Heather Walters of CRB spends her time thinking about effective business and industrial sustainability and resource conservation. Meanwhile, Chief Editor Louis Garguilo maintains a position near the bottom of the list of interested parties. It made for great conversation. Uncovered were the current realities of sustainability in manufacturing facilities, and the importance of two components: electrification and digital twins.

The 2026 Pharma R&D AI Sourcing Map: Partnerships, Concentration, Inflection

A Beroe analysis of 2026 pharma AI deals shows discovery still dominates, suppliers are consolidating, and clinical development is the next AI sourcing frontier.

INDUSTRY INSIGHTS CONTINUED

Imprints On Oral Solid Dosage Forms

Selecting the right tablet imprinting technology is essential for product identification and compliance. Improve your print clarity, speed, and overall manufacturing efficiency.

Beyond Compliance: What Defines Quality Excellence In A CDMO

Strong quality programs are built on more than audits. Explore how culture, systems, and continuous improvement support reliable manufacturing outcomes.

Advancing Corticosteroids And Hormonal Therapies For Supply And Scale

Tune in to discover the science, strategy, and manufacturing expertise behind the steroid and hormonal therapies that improve millions of lives worldwide.

AAPS PharmSci 360 2026: Formulation Partnerships With Mikart

A preview of AAPS PharmSci 360 2026 highlighting formulation science, patient‑centric oral dosage forms, and strategies for translating early research into scalable, manufacturable drug products.

Safely Scaling High Potency API Manufacturing

Scaling HPAPI production demands disciplined containment and exposure control. Integrated operating models help manage risk while enabling compliant, reliable scale‑up.

Reshaping Drug Development With 3D Screen Printing

Steven Facer and Laxxon Medical COO Klaus Kühne describe the capabilities of 3D screen printing for pharmaceutical production. Explore prototyping, IP protection, release profile possibilities, and more.

75 Years Of Growth, Values, And Global Supply Resilience

Global expansion and supply chain flexibility are reducing risk and strengthening continuity. See how a multi-site strategy supports quality and customer success worldwide.

SPONSOR

Enabling ADC Success | Dec. 1, 2026, 11:00 AM ET

This session explores the development, analytical, and manufacturing strategies supporting antibody-drug conjugate (ADC) and emerging conjugate programs. CDMOs will discuss challenges related to conjugation, CMC, developability, lyophilization, and complex payloads, including antibody-oligonucleotide conjugates. Attendees will gain insights into early risk mitigation, optimization strategies, and science-driven approaches that help improve program success and support efficient development and manufacturing. Learn more.

SOLUTIONS

Sterile Steroid APIs: What The Valladolid Site Is Built To Handle

Custom API Manufacturing From Early Development To Commercial

How AI Is Transforming Solid-Form Screening In Drug Development

Regulatory Starting Materials (RSMs) — India

Drug Product Formulation And Manufacturing

OUTSOURCED PHARMA CAPABILITIES UPDATE

Find Your New CDMO At Outsourced Pharma Capabilities Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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