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Quality

GC Biopharma produces
Reliable products with
Robust quality control in compliance
With global GMP standards.

Maintaining a robust quality system,
we uphold intensive internal policies and procedures.

To establish a quality system that
satisfies domestic and international regulatory requirements,
the Quality Code of Quality (CQM) was enacted.
This code outlines a consistent and standardized level of quality.

Quality Assurance

Quality Assurance

We are responsible for
establishing standards to
ensure that all products and
services are manufactured,
tested, released, and
distributed in compliance
with regulatory requirements.
We continue to ensure
ongoing compliance with GxP
to improve these standards.

Quality Control

Quality Control

The quality testing of the
manufactured product is
conducted independently, and
the reliability of these quality tests
is ensured by performing AMV
(Analytical Method Validation).

Quality Risk

Quality Risk

We evaluate and monitor
the safety of our products
via clinical and non-clinical trials.
This helps ensure drug
safety and development in
compliance with regulations.
We strive to provide
our customers with only
the highest quality of products.

Quality Monitoring System

Quality Monitoring System

We comply with
reporting obligations under
regulatory pharmacovigilance
agencies for all adverse events
related to the use of our products.

이메일집단수집거부

GC녹십자는 이메일 수집을 거부합니다

본 웹사이트에 게시된 이메일 주소가 전자우편 수집 프로그램이나
그 밖의 기술적 장치를 이용하여 무단으로 이메일 주소를 수집하는 행위를 거부하며,
이를 위반시 정보통신망 이용촉진 및 정보보호 등에 관한 법률에 의해 형사처벌됨을
유념하시기 바랍니다

게시일: 2003년 9월 1일