Newsletter | October 2, 2024

10.02.24 -- Sanofi, Sanctions, And Supply-Chain Challenges

SPONSOR

Supporting Your Solid Formulation with Functional Excipients for Optimal Performance

Solid dose formulations are one of the most established dosage forms in pharmaceuticals. However, there are many challenges in their design, such as API stability, release kinetics or bioavailability limitations. With our comprehensive range of functional and particle-engineered Parteck® excipients, we’re here to meet your needs and help you ensure optimal performance in your formulation development and manufacturing. Learn more about our functional excipients

FEATURED EDITORIAL

Sanofi, Sanctions, And Supply-Chain Challenges

In part one, we met Arezou Mehrabi. Now, she shares a case study of a supply chain challenged by trade sanctions, and how Big Pharma (Sanofi) collaborated with a CMO to keep delivering essential medicines. Set in Iran, circa 2018, it's a lesson for all outsourcers provided by the woman who led the charge to get manufacturing back on track.

Araris Doubles Down With Dual-Payload ADC

Antibody-drug conjugates usually deliver one payload type, which can overlook cancer’s complexity. A single ADC delivering two separate payloads could be the answer.

The Key Questions Of Strategy For Outsourcing

Chief Editor Louis Garguilo kicks off this virtual event by highlighting key questions to ask about the strategic direction of drug development and manufacturing outsourcing.

INDUSTRY INSIGHTS

How Approved Drugs Have Evolved Since The '70s

Drugs have become more lipophilic and complex in structure over time. Innovative strategies are needed to improve bioavailability of these new drugs.

Recent Innovations And Enhancements To Pharmaceutical Spray Drying

Alternative solvent approaches could reduce volumes of less toxic solvents, significantly improving the environmental and human health impacts of new drugs.

Zydis Orally Disintegrating Tablet (ODT) Vs. Standard Tablets (ST)

See how Zydis ODT compares to standard oral tablets, how the same molecule can produce different outcomes when utilizing Zydis ODT, and findings from over 20 studies.

Leveraging Tools To Create Optimized Solutions

Review key trends and challenges in the CDMO industry and the tools helping to meet the demand for pediatric formulations and taste-masking solutions.

Investing In Capacity – API Commercial Manufacturing

A pharma company sought a CMO partner with commercial manufacturing capabilities and expertise as well as exemplary quality systems to find a cost-effective process to produce the API for a new drug.

SPONSOR

Join the next Outsourced Pharma Live as our panel explores the critical considerations and best practices for selecting and managing CDMOs in the development of novel therapies, including advanced therapy medicinal products like cell and gene therapies. Industry experts will share insights on evaluating CDMO capabilities, ensuring quality and compliance, and fostering effective partnerships to accelerate innovation while mitigating risks.

SOLUTIONS

Pharmaceutical Contract Packaging And Filling Services

With ample available capacity, we provide the efficiency of five bottling lines with quick changeovers, online validated fill accuracy, and the flexibility to accommodate small lots to commercial runs for tablets, capsules, and powders.

Capacity Update July 2024: Small Molecule Finished Dosage Form

We specialize in high-potency softgels and liquids and have deep experience producing prescription drugs for classifications including oncology, dermatology, the central nervous system and immunity.

OUTSOURCED PHARMA CAPACITY UPDATE

Find Your New CDMO At Outsourced Pharma Capacity Update

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

Connect With Outsourced Pharma: