Newsletter | May 8, 2024

05.08.24 -- You Want To Rein In China? Then Actually Do It

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Showcasing state-of-the-art facilities and cutting-edge equipment driving the API manufacturing process - Outsourced Pharma Capacity Update’s new PARTNER WEEK offers an extended schedule grouped by capability including a new Small Molecule API & HPAPI Development session. Register today for this digital event happening May 22nd.

FEATURED EDITORIAL

You Want To Rein In China? Then Actually Do It

Our team of analytical experts provides experience, efficiency, and technical proficiency in the development/validation of analytical methodology and GMP testing support.

The EU’s Ban On TiO2 In Food May Impact Pharma. Here’s What To Know.

Titanium dioxide (TiO2) is used as a food additive and OSD pharmaceutical excipient. In 2020, the European Food Safety Authority noted data gaps regarding particle size, which can affect its toxicological properties, so the European Commission banned it as a food additive. Here's how this could impact pharma.

INDUSTRY INSIGHTS

Ophthalmic Drug Delivery

Explore the challenges to effective delivery of drugs to the eye, the intricacies of ophthalmic drug delivery, and the advantages of nanoparticles as an enabling technology for ocular drug-delivery systems.

Supply Chain Sustainability: Manufacturing Of RSMs And KSMs

De-risking RSM and KSM procurement can be accomplished via several means, but local sourcing of raw materials and in-house production have proven tremendously effective.

Improving An Abandoned Medication Using Innovative ASD Technology

Review the case study and learn how improved solid dispersion lowered patients' pill burdens and demonstrated an improved therapeutic response for Galeterone.

Simultaneous Spray Drying: Dry Powder Inhaler Combination Formulations

The simultaneous spray drying of multiple ingredients is a powerful technique for making inhaled products with multiple actives. Examine how novel techniques can make these products a reality.

SOLUTIONS

R&D And Analytical Services

Our team of analytical experts provides experience, efficiency, and technical proficiency in the development/validation of analytical methodology and GMP testing support for your project.

Biocatalysis For Cost-Efficient, Environmentally Friendly Manufacturing

Biocatalysis enables cost efficient and environmentally friendly manufacturing through enzymatic synthesis and provides pure -regio, chemo- and enantioselective compounds when compared to traditional chemical synthesis.

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.

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