What We Offer
Litamar provides three core service lines to pharmaceutical companies, distributors, and healthcare organizations worldwide. Each service is underpinned by rigorous quality standards and a commitment to precision manufacturing.
Encapsulated Products
Precision dosing in every capsule.
Our encapsulation capabilities cover both hard and soft gelatin capsules across a comprehensive range of therapeutic categories. We work with pharmaceutical-grade excipients and active pharmaceutical ingredients (APIs) to deliver consistent, precisely dosed products that meet international quality standards.
- Hard gelatin capsule filling (sizes 000 to 5)
- Soft gelatin capsule manufacturing
- Immediate and modified-release formulations
- Powder, pellet, and liquid fills
- Custom color and branding options
- Full batch documentation and CoA
Sterile Production
Aseptic manufacturing to the highest standards.
Our sterile production facilities operate under ISO-classified cleanroom conditions with rigorous environmental monitoring. We specialize in aseptic fill-finish operations for injectable products, ensuring the highest levels of sterility assurance and product integrity throughout the manufacturing process.
- ISO Class 5/7/8 cleanroom environments
- Vials, ampoules, and prefilled syringes
- Lyophilization (freeze-drying) capability
- Continuous environmental monitoring
- Full sterility testing and endotoxin testing
- Regulatory-compliant batch records
Private Label
Your brand, our manufacturing excellence.
Litamar's private label service provides a complete end-to-end solution for organizations seeking to bring branded pharmaceutical products to market. From initial formulation development and stability studies through regulatory documentation and branded packaging, we manage the entire process.
- Formulation development and optimization
- Stability studies and shelf-life determination
- Regulatory dossier preparation
- Custom packaging and label design
- Distributor network support
- Post-market surveillance support
Our Process
Initial Inquiry
Submit your requirements via our inquiry form or email. Our team reviews your needs within 24–48 hours.
Consultation
We connect you with the appropriate manufacturing partner and discuss specifications, volumes, and timelines.
Documentation
Regulatory documentation, quality agreements, and production specifications are finalized and agreed upon.
Production & Delivery
Manufacturing proceeds under GMP conditions with full batch documentation and quality release before shipment.