Attending RDD 2026? Meet our team in Phoenix, Arizona, during the conference to discuss all aspects of pulmonary and nasal drug delivery development challenges

Join our team at the Respiratory Drug Delivery (RDD) 2026 Conference (May 10–14, Phoenix, Arizona) to discuss the latest challenges and innovations in pulmonary and nasal drug development.

Get in touch with our team now - We’ll be available throughout the event to explore your OINDP development programmes, including:

Our experts will also be sharing updates on the commissioning of our new GMP facility in Melbourn, Cambridge (UK), adding 29,000 sq ft of manufacturing and analytical capacity. Designed to support next-generation inhaled and nasal therapies, including biologics for respiratory delivery, this expansion enables parallel clinical manufacturing campaigns with the flexibility to adapt to evolving programme needs.

Backed by integrated formulation, analytical, and manufacturing teams, we support development from early pre-formulation and solubility screening through to device selection, stability studies, and GMP clinical manufacturing. Our capabilities also include comprehensive protein characterisation, ensuring critical quality attributes such as structure, stability, and potency are maintained throughout development.

Get in touch to arrange a meeting in Phoenix and explore how we can support your programme from concept to clinic.

Latest respiratory drug delivery resources: 
Guide: Key Considerations for Developing Intranasal Nucleic Acid Therapies for CNS Targets
Our experts provide a concise overview of the key challenges and emerging opportunities in developing intranasal delivery strategies for mRNA and oligonucleotide therapeutics targeting the central nervous system.

Q&A: Building Flexibility into the Future of Next Generation Therapies: Expanded CTM Manufacturing and Integrated Analytical Resources
This expert interview with Teresa Iley, our Director Pharmaceutical Development & Manufacturing, explores how greater flexibility can be integrated into the development of inhaled and nasal drug products to address increasing complexity in formulation, device design, and regulatory expectations.

Missed our RDD Europe 2025 Conference Poster?
This study looked at both currently marketed subcutaneous injection formulations and prototype formulations to investigate the effect of higher drug loading. here: Aerosolization of Wegovy® and Prototype Formulations of Semaglutide with MRX004 SMI

BROCHURE | Intertek Inhaled Product Development Services 
BROCHURE | Inhaled Biologic Drug Development Services

 

Need help or have a question?

Related Links

Intertek Melbourn Laboratory

GMP Pharmaceutical Analysis and Formulation Expertise

Intertek Melbourn
Saxon Way, Melbourn
Herts, SG8 6DN 
UK

RECENT NEWS: Intertek partners with CrystecPharma to advance formulation science and accelerate development for dry powder inhalers

The Inhaled and Nasal Biologics DNA forum logo in white and yellow font against a dark turquoise backgrouns

5th Annual Inhaled & Nasal Biologics | DNA Forum

24-25 September 2026 
Cambridge, UK 


Join us for a ground-breaking and insightful forum on inhaled and nasal biologics development: Two days of cutting-edge talks and networking opportunities with leaders in this complex area of inhaled medication and inhaled vaccine development.
LEARN MORE & REGISTER

Contact Intertek