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科典醫藥生技 GMP 認證工廠外觀 | CODAN Biotech GMP Certified Factory
Factory Introduction

Factory Introduction

Why Choose CODAN?

Factory Introduction

Dust-Free Factory Area, Benchmarking Pharmaceutical Standards

We have established a dust-free area that meets the SGS-tested Class 10,000 cleanroom standard. This cleanroom standard actually meets the regulatory requirements for manufacturing non-sterile pharmaceuticals.

To reduce cross-contamination, the factory area is equipped with buffer zones to ensure that the cleanroom environment is not affected by incoming materials. Finished products from the production area are transported to the packaging room via transfer boxes. Additionally, all personnel entering or exiting the cleanroom must wear dust-free clothing, which is regularly cleaned and replaced according to the dress code.

The walls of the cleanroom are made of anti-static materials, and the floor is effectively grounded to dissipate static electricity. Each factory compartment is equipped with temperature and humidity monitoring equipment to ensure that products are manufactured in a controlled environment with constant temperature and humidity.

High-Level Cleanliness & Regular Maintenance

Our facility undergoes daily disinfection and cleaning, with routine airborne microbial testing to ensure a pristine cleanroom environment. Additionally, we partner with licensed pest control and sanitation specialists to conduct comprehensive facility-wide disinfection on a scheduled basis. This ensures optimal hygiene standards and a safe production environment.

 GMP cleanroom disinfection and maintenance, ISO 22716 certified facility with microbial monitoring and professional pest control for hygiene safety

Pharmacist R&D, Professional Supervision

CODAN employs a team of licensed pharmacists responsible for formula design. With their expertise in pharmacology and pharmaceutics, they are able to create scientifically sound and safe formulas tailored to the needs of contract manufacturing, ensuring that the product’s texture, stability, and efficacy meet the expected standards.

Pharmacist-developed skincare formulations, professional supervision ensuring stability and safety, compliant with GMP and ISO 22716 standards

Integrated PIF, One-Stop OEM

After product manufacturing is completed, CODAN employs professionally trained and certified technical production personnel and Safety Data Signatories (SA) who can assist clients in establishing the Cosmetic Product Information File (PIF). This eliminates the need for clients to spend time seeking separate PIF documentation services, offering a true one-stop experience for skincare product contract manufacturing.

Professional technicians in one-stop skincare OEM service, helping clients establish the Product Information File (PIF) without the need for additional third-party services, offering a complete service experience.