Cosmetic Product Development Process in Korea

At this stage, we want to understand: your target market, preferred product category, approximate order scale, desired positioning (mass, mid-range, premium), and any ingredient preferences or restrictions.

We recommend choosing at least one clear target product. If the lab only receives vague descriptions like "premium texture" or "glass skin," the first sample will almost certainly miss the mark. A physical reference product removes ambiguity.

This is where we align on the formula architecture. We confirm whether you want specific actives (Niacinamide, Retinol, Vitamin C, peptides), the desired viscosity, the skin feel after absorption, and whether the product needs to meet specific market regulations.

The lab formulates the base, adjusts the texture, and incorporates the agreed actives. You receive a small batch for evaluation — usually 50–200g depending on the product type.

This is an iterative process. Most projects require 1–3 revision rounds before the formula is approved. Clear, specific feedback ("I want it to absorb faster" or "I want a more matte finish") leads to better results than vague reactions.

Packaging options include airless pumps, glass droppers, tubes, jars, and custom molds. We advise on material compatibility — certain ingredients degrade in contact with specific plastics or metals.

Compatibility testing typically runs for 1–2 months at various temperatures. This ensures the formula remains stable, the packaging does not degrade, and the dispensing mechanism works correctly throughout the product shelf life.

Production MOQ varies by product type and manufacturer. We coordinate production scheduling, monitor quality control checkpoints, and ensure batch consistency meets the approved sample standard.

Depending on your market, you may need CPNP notification (EU), FDA facility registration (US), or ASEAN compliance documentation. We guide you through what is required and help compile the necessary paperwork.