Terms of Service

These Terms of Service govern all contract manufacturing agreements, formulation consultations, label design collaborations, packaging procurement, and global distribution licensing operated by Marinas International USA LLC. By submitting an inquiry or executing a production order, you legally agree to these guidelines.

Marinas specializes in transforming client concepts into clinical-grade supplements using high-end, premium ingredients. We guarantee production in modern, FDA and GMP-compliant facilities in the USA. Formulas may be custom-engineered by our Ph.D. chemists or selected from our scientifically tested catalog.

Standard production cycles run on highly competitive 4 to 8-week timelines following formal label and raw material sign-offs. Any delay in client-submitted designs, active ingredients approval, or deposit execution may adjust target fulfillment schedules proportionally.

Every manufactured batch undergoes rigorous QA review and independent lab testing to verify microbiological purity and label accuracy. Clients are responsible for ensuring that custom ingredients and visual label health claims comply fully with state, federal, or destination-country regulations.

Quotes are customized based on production size, component sourcing, and packaging complexities. Unless noted otherwise in a specific master services contract, raw ingredient procurement begins immediately upon receipt of a standard 50% deposit, with the remainder due upon final batch QA certification.

These terms, along with all master manufacturing contracts, are executed and governed by the laws of the State of Wyoming, USA, or international legal frameworks corresponding to specific Marinas regional distribution nodes. Any arbitration or claims must be submitted to our designated judicial forums.