Turnkey Contract Manufacturing Excellence
Vovantis operates as a full-spectrum CDMO partner — from formulation development and regulatory filing through commercial-scale manufacturing, primary packaging, and global logistics. We offer both technology licensing and white-label private label manufacturing with complete IP confidentiality.
Our vertically integrated campus in Ranoli, Vadodara houses dedicated effervescent, solid oral dosage, and sachet manufacturing suites with automated high-speed production lines, inline quality controls, and moisture-barrier packaging infrastructure.
End-to-End Manufacturing Solutions
From molecule to market — our integrated CDMO platform accelerates your product launch across regulated global markets.
Custom Formulation Development
Proprietary effervescent, tablet, capsule, and sachet formulation development from pre-formulation through pilot-scale validation.
Commercial-Scale Manufacturing
High-speed automated production across effervescent tablets, conventional tablets, hard capsules, and dry powder sachets with inline quality controls.
Primary & Secondary Packaging
Moisture-barrier Alu-Alu blisters, desiccant tubes, multi-laminate sachets, and carton labeling with serialization and track-and-trace readiness.
Private Label & White Label
Complete private-label manufacturing with your brand identity — from artwork design through final packaged goods ready for distribution.
Regulatory & Dossier Support
CTD/eCTD preparation, stability programs (ICH Zones I–IVb), Drug Master Files, and Site Master Files for global health authority submissions.
Supply Chain & Global Logistics
Temperature-controlled warehousing, export documentation, and logistics coordination to 30+ international markets with full chain-of-custody traceability.
Engagement Workflow
Our structured CDMO engagement model ensures complete transparency, milestone-driven deliverables, and on-time market entry.
Technical Feasibility & NDA
Phase 01: ScopingInitial project scoping, mutual NDA execution, API compatibility assessment, and preliminary cost and timeline estimation.
Formulation & Prototype
Phase 02: Lab FormulationCustom formulation development, trial prototype preparation, organoleptic optimization, and preliminary stability evaluation.
Pilot Batch & Validation
Phase 03: Scale-Up & Tech TransferScale-up to pilot batches under low RH climate controls, process validation, analytical method validation, and regulatory dossier preparation.
Commercial Launch
Phase 04: cGMP Global ReleaseFull-scale commercial manufacturing, automated packaging with 2D DataMatrix serialization, quality release, and global export coordination.
Ready to Launch Your Product Globally?
Our CDMO team is ready to evaluate your project, propose competitive terms, and deliver commercial-ready products with complete regulatory dossier support.