Liquid / Syrup Manufacturing

Oral liquids, syrups, suspensions, and elixirs manufactured in cGMP compliant liquid manufacturing units with fully automated filling lines.

Why Choose Arbro's Liquid / Syrup Manufacturing?

• WHO-GMP and ISO 9001:2015 certified manufacturing facility
• 40+ years of pharmaceutical manufacturing expertise
• In-house R&D for formulation development and optimisation
• Dedicated quality control team with in-process testing
• Full batch documentation and regulatory compliance
• Flexible batch sizes and competitive pricing
• Dedicated project manager for your account

Our Liquid / Syrup Manufacturing Process

1. Enquiry & Consultation — Share your product specifications. We review and respond within 48 hours with a detailed proposal.
2. Formulation Review / Development — Our R&D team reviews your existing formulation or develops a new one tailored to your requirements.
3. Process Development & Scale-up — Laboratory batches are scaled to commercial production with documented process parameters.
4. Manufacturing — Production in our WHO-GMP facility with real-time in-process quality monitoring.
5. QC Testing & Release — Comprehensive quality control testing, CoA generation, and batch release by our QA team.
6. Packaging & Delivery — Branded packaging as per your specifications and timely delivery to your location.

Manufacturing Certifications

All products manufactured at Arbro Pharmaceuticals comply with:

• WHO-GMP (World Health Organization Good Manufacturing Practice)
• ISO 9001:2015 Quality Management System
• Schedule M – Drugs and Cosmetics Act, India
• FSSAI (for nutraceutical products)
• AYUSH (for Ayurvedic/herbal products)