07.02.25 -- Scaling Up Manufacturing? Here's Why You Need A CMC Specialist

Dry powders for inhalation (DPIs) represent a versatile delivery platform. However, there are key factors such as required dosage and desired release profiles that dictate the development approach for DPIs. Join Lonza for a webinar that will highlight the key aspects in the product development of inhalation and nasal dry powder products from a CDMO perspective. Click here to learn more.

Navigate the complex IND process with expert guidance and discover how early FDA engagement can accelerate your path to clinical trials.

Whether working with small-scale formulations or preparing for commercial manufacturing, this session will provide actionable strategies to optimize development pipelines.

Drug developers and manufacturers must address several key challenges, including formulation complexity, improving bioavailability of poorly soluble compounds, and optimizing drug release profiles.

CMC experts (whether in-house or outsourced) fill a vital role during the transition from small-scale production to larger operations for maintaining quality, consistency, and compliance.

A focus on spray-drying expertise in pulmonary and nasal powder development highlights why it is vital to choose the right CDMO.

Explore the transformative potential of pharmaceutical spray drying in improving drug formulation, bioavailability, and delivery through versatile and innovative applications.

Spray dry technology is being leveraged to create shelf-stable, dry-powder vaccines to treat and prevent the spread of tuberculosis which could significantly improve our global response to disease.

20-minute capacity and capabilities quick-looks, 20+ brand new CDMO presenters to evaluate for best-fit this quarter – and a (virtual) commitment of less than 20 percent of your day? We're confident you don’t need 20/20 vision to see the value in this! Join us for Outsourced Pharma's July Partner Week – including sessions in Small Molecule API/HPAPI, Small Molecule Finished Dosage Form, ADC, Analytical Services, and Fill/Finish among others. Registration, on-demand access, and interactive Q&A are free.

Discover an analytical laboratory seamlessly integrated with manufacturing and packaging operations, which offers dependable chemical and microbiological testing that adheres to cGMP standards.

The Pharma Expanse network currently spans across 9 manufacturing sites in 5 countries and can support discovery, preclinical, clinical and commercial programs for New Chemical Entities (NCEs). Pharma Expanse has an innovative business model that does not add additional costs to your project. Review our network's process development and preclinical manufacturing capabilities below and contact us to simplify your outsourcing solutions.

Gain insight into the capabilities of our award-winning development and manufacturing facility, which features 10 state-of-the-art GMP manufacturing suites integrated with cutting-edge R&D and QC laboratories.