2025 Partners
Aptar Pharma
Expertise Partner
Aptar Pharma is an expert in nasal drug delivery, offering advanced intranasal systems and drug delivery services from design and manufacture, formulation development and clinical product manufacturing to post launch support. Our global network of GMP manufacturing sites help us accelerate and derisk drug product development, and our investments in R&D and innovation allow us to offer proven nasal drug delivery solutions to help improve patient outcomes across the globe.
Renaissance Lakewood
Expertise Partner
Renaissance Lakewood, LLC is a US-based contract development and manufacturing organization (CDMO) for pharmaceutical and biotech companies. With more than 20 years of experience in nasal sprays and sterile injectable dosage forms, Renaissance has an established track record of providing exceptional service and resources to clients from the product development stage through commercial manufacturing.
Silgan Dispensing
Expertise Partner
Silgan Dispensing Systems is a specialized pharmaceutical packaging and dispensing systems provider with a global manufacturing presence and an extensive line of high quality solutions that do more than simply protect medicine. We collaborate with customers, fillers, machinery manufacturers, retailers and other partners to accelerate commercialization of consumer-centric packaging solutions. We are proud to serve patients’ needs, from topical to ophthalmic to throat to ear to nasal; our dispensing solutions are designed to provide the best patient experience.
Nemera
Expertise Partner
As a world-leading drug delivery device solutions provider, our purpose of putting patients first enables us to design and manufacture devices that maximize treatment efficacy. We are a holistic partner and help our customers succeed in the sprint to market of their combination products. From early device strategy to state-of-the-art manufacturing, we’re committed to the highest quality standards.
Agile and open-minded, we work with our customers as colleagues. Together, we go the extra mile to fulfill our mission.
To know more, visit: www.nemera.net
MedPharm
Exhibition Partner
MedPharm: Leading Topical and Transdermal Drug Development
Founded in 1999 out of King's College London, MedPharm has grown into a premier end-to-end contract development and manufacturing organization (CDMO) specializing in topical, transdermal, and transepithelial pharmaceutical products. With facilities in Guildford, UK, and Durham, NC, USA, we provide comprehensive services spanning formulation, analytical development, in vitro testing, clinical trial material supply, and commercial manufacturing.
Renowned for our expertise in semi-solid and liquid formulations, MedPharm supports clients across more than 30 countries. Our proprietary technologies and innovative in vitro models expedite development timelines, reduce risk, and provide unparalleled insights into drug efficacy and delivery. From addressing complex delivery routes—such as dermal, nasal, and ocular—to shipping FDA-approved commercial products, MedPharm offers a seamless pathway from concept to market.
With a commitment to quality and regulatory excellence, we’ve facilitated the development of over 80 commercial products and continue to push the boundaries of pharmaceutical science. MedPharm's dedication to precision, innovation, and collaboration ensures your product's success at every stage of development.
For more information, visit medpharm.com.
Intertek
Event Partner
Our 30 years of experience in formulation and nasal drug development support can drive the insight you need to develop advanced drug delivery systems for targeted and controlled release of novel therapies or vaccines. With specialist expertise in orally inhaled & nasal drug product development across both large and small molecules, we provide analytical development, integrated with formulation and stability to drive understanding of our clients’ products and processes, enabling our clients’ key decision-making activities including performance testing, method development/validation, stability, E&L, CMC support, formulation development, repurposing and clinical manufacturing capabilities.
Across the product development lifecycle for both biologics and pharmaceuticals. We offer a broad range of analytical services including characterisation for biologics, DNA therapies, peptides, cell and gene therapies, liposome, LNP and nano-particle technologies alongside solubility, dissolution, particle morphology (Malvern Morphologi 4 ID) and other inhaled delivery performance aspects (delivered dose, aerodynamic droplet size distribution, spray pattern etc).
- Method Development / Validation
- Analytical Testing
- Formulation Development
- Device Screening
- Quality by Design (QbD) Studies
- ICH and Accelerated Stability Studies
- In-Vitro Bioequivalence Studies (IVBE)
- Clinical Trials Materials Manufacturing
- Product Characterisation Studies
- Biologics Characterisation
