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Quality

GC Biopharma produces
Reliable products with
Robust quality control
Compliance to global GMP

Maintains Robust Quality System with
Intensive Internal Policies and Procedures

In an effort to establish a quality system that
satisfies domestic and international regulatory requirements
the Quality Code of Quality (CQM) was enacted,
which defines a consistent and standardized quality level.

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
continued compliance with GxP
to improve these standards.

Quality Control

Quality Control

The quality test of the
manufactured product is
carried out on its own, and
the reliability of the quality test
is secured by performing AMV.
(Analytical Method Validation).

Quality Risk

Quality Risk

We evaluate and monitor
the safety of our products
through non-clinical and
clinical trials to ensure drug
safety and develop in
compliance with regulations.
We are doing our best to
ensure that high-quality
products are delivered
to customers.

Quality Monitoring System

Quality Monitoring System

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

이메일집단수집거부

GC녹십자는 이메일 수집을 거부합니다

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이를 위반시 정보통신망 이용촉진 및 정보보호 등에 관한 법률에 의해 형사처벌됨을
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게시일: 2003년 9월 1일