Nasal Spray OEM Programme
ShiLai™ Healthcare's nasal spray OEM programme supports B2B partners in developing peptide nasal spray products for research supply. The programme covers the full development workflow from initial formulation through to finished, labelled product.
All products are developed and supplied for research purposes. No therapeutic claims are made. OEM partners are responsible for compliance with applicable regulations in their jurisdiction.
OEM Development Workflow
01
Project Brief
Submit your peptide, target format, volume requirements, and intended research application.
02
Formulation Consultation
Buffer system, pH, preservative, and isotonicity assessment for your peptide and delivery format.
03
Device Selection
Nasal spray actuator and container selection based on formulation compatibility and dose requirements.
04
Prototype Development
Fill-and-finish of prototype batches for analytical testing and client review.
05
Analytical Testing
Purity, potency, and stability testing on prototype batches. COA provided.
06
Packaging Integration
Label design, secondary packaging, and private-label integration for qualified OEM clients.
Nasal Spray Private Label
Private-label nasal spray development is available for qualified OEM clients. This includes custom label design, secondary packaging integration, and brand-specific packaging formats. Minimum order quantities and lead times are defined per project.
Private-label products are supplied for research and development purposes only.
Packaging Integration
Packaging integration for nasal spray OEM products includes primary container labelling, secondary carton design, and batch documentation. All packaging is produced to GMP standards.
Project Inquiry Requirements
To initiate an OEM nasal spray project discussion, the following information is typically required:
- Molecule or formulation
- Intended format (single-chamber, dual-chamber, cartridge)
- Target fill volume
- Device preference
- Cartridge requirements
- Packaging requirements
- Target market
- Estimated quantity
- Documentation requirements
Project feasibility, timelines, and specifications are assessed on a per-project basis. No guaranteed launch, regulatory approval, clinical outcome, delivery date, absorption, or therapeutic benefit is implied.
All OEM nasal spray products are developed and supplied for research and development purposes. OEM partners are responsible for compliance with applicable regulations in their jurisdiction. Target market and compliance review is part of the project discussion process.
Submit a Project Brief
Contact us via WhatsApp to discuss your nasal spray OEM or private-label project requirements.
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