OEM/ODM

ODM (Original Development & Design Manufacturing)

ODM is a service provided by a company (manufacturer) capable of designing and manufacturing products according to the specifications required by the Seller (Brand). Kolmar does not merely provide basic ODM services (processing and production); we provide a comprehensive ODM solution, from concept consulting, product development, and manufacturing to complete licensing and shipping services.

Market Research

Concept Development & Planning

Made in Korea (Manufacturing in Korea)

Import & Delivery

Product Registration & Licensing

Complete ODM
Process

Do you have an idea for a cosmetic or pharmaceutical product and need a reputable ODM partner? Kolmar Korea – South Korea's leading ODM group – provides a comprehensive end-to-end service from concept to production. With in-depth experience and market trend insights, we support planning, R&D, and manufacturing, ensuring a finished product is delivered to your customers.

Global Quality Framework

Quality Principles

- An integrated quality policy based on global standards
- Management of quality accountability indicators (KPI) across all global sites in line with our Quality First philosophy
- Application of Design by Quality, ensuring quality is built into products from the development stage

Global Quality Framework

Global Standard Quality System

- Application of global standards for core processes and quality control through SOPs (Standard Operating Procedures)
- Unified production and testing operations based on CGMP and ISO requirements, including harmonized test methods and inspection criteria

Global Quality Framework

Risk Management

- Operation of a globally integrated risk management process
- Global escalation flow: Local QA → Global (GAO) QA → Headquarters
- Systematic response to quality issues through root cause analysis, improvement actions, and effectiveness verification based on impact, severity, and scope Transparent, customer-centric communication

Global Quality Framework

Continuous Quality Capability Enhancement

- Establishment of a compliance framework aligned with global regulations, including ISO, FDA, Health Canada, and NMPA
- Enhancement of supply chain quality through a global supplier quality audit system
- Operation of global quality training programs across all sites, covering QA, QC, R&D, and manufacturing