Suspension Manufacturing
Advanced CDMO solutions for regulated oral suspension formulations. End-to-end third party pharmaceutical manufacturing with scalable liquid dosage production.
Comprehensive Oral Suspension Manufacturing Services
Suspension manufacturing requires precise particle size control, uniform dispersion, and validated mixing systems to ensure dose accuracy and stability. As a pharmaceutical suspension manufacturer, Delwis delivers compliant third party pharmaceutical manufacturing solutions for a wide range of oral liquid dosage forms. Our facilities are engineered to support oral suspension manufacturing services aligned with regulated market expectations.
We provide scalable, quality-driven CDMO partnerships for pharmaceutical companies seeking reliable and long-term suspension manufacturing support.
Quality
Oral suspension manufacturing demands strict control over particle size distribution, sedimentation stability, and microbial limits. Our WHO-GMP aligned facilities ensure consistent mixing, accurate filling, and contamination-free processing environments. Every batch undergoes comprehensive in-process controls and finished product quality testing prior to release.
- WHO-GMP compliant suspension manufacturing facilities
- Validated dispersion and homogenization systems
- In-house analytical and microbiological testing laboratories
- Controlled water purification and sanitation systems
- Complete batch traceability and documentation protocols
Our Approach
We combine formulation expertise with commercial scalability to deliver reliable oral suspension manufacturing services. Our third party pharmaceutical manufacturing model ensures seamless technology transfer, validated scale-up, and predictable supply performance.
Augmented Services Along With Quality Medicines
Beyond suspension manufacturing, we deliver regulatory and operational support that strengthens commercialization. Our third party pharmaceutical manufacturing framework ensures compliance, quality, and supply reliability.
Regulatory Dossier Support
Comprehensive documentation aligned with domestic and global regulatory standards.
Technology Transfer Management
Structured onboarding for compliant suspension product transfer.
Stability Programs
Accelerated and real-time studies ensuring suspension shelf-life validation.
Bottle Filling & Packaging
Precision filling with tamper-evident, export-ready packaging solutions.
Why Delwis
Delwis stands as a trusted CDMO partner for companies seeking dependable oral suspension manufacturing services. Our operational discipline, regulatory alignment, and scalable infrastructure support confident outsourcing decisions.
Whom We Work With
We collaborate with pharmaceutical organizations seeking compliant and scalable CDMO partnerships for suspension manufacturing. Our model supports both emerging and established brands.
Our Ideal Partners
Pharmaceutical companies expanding oral liquid portfolios
Global firms seeking third party pharmaceutical manufacturing partnerships
Organizations requiring compliant CDMO scale-up solutions
Export-focused companies targeting regulated markets
| Product Name | Composition | Class | |
|---|---|---|---|
| Delcold Plus Susp | Anti Cold C.P.Maleate 2mg + Paracetamol 250 mg + Phenylephrin HCl 5mg Susp | Suspensions, Antiasthmatics / Neurolytic / Antiallergic | Details |
Start Your Suspension Manufacturing Project
If you are looking for a reliable pharmaceutical suspension manufacturer offering compliant oral suspension manufacturing services, Delwis Healthcare is ready to support your third party pharmaceutical manufacturing requirements.
No form fields available.
FAQs
Below are common questions from pharmaceutical companies evaluating our CDMO and third party pharmaceutical manufacturing capabilities for suspension formulations.