홈

적격성평가

설비 및 시설 적격성평가(IQ/OQ/PQ).

GMP
적격성평가
2026년 8월 24일
Autoclave Qualification — Thermal Distribution and Penetration Studies
How thermal distribution and penetration studies qualify an autoclave for reliable sterilization.
1
GMP
적격성평가
2026년 8월 24일
Computerized System Qualification — Integration with CSV Lifecycle
How equipment qualification and computer system validation activities are coordinated for integrated systems.
GMP
적격성평가
2026년 8월 24일
Design Qualification (DQ) — Approach for New Manufacturing Equipment
How Design Qualification confirms proposed equipment design meets user and regulatory requirements before purchase.
GMP
적격성평가
2026년 8월 24일
HVAC Qualification — Airflow and Particle Count Verification
How airflow velocity, air changes, and particle counts are verified to qualify an HVAC system.
1
GMP
적격성평가
2026년 8월 24일
Installation Qualification (IQ) Protocol — Structure and Content
What a well-structured IQ protocol covers, from documentation checks to utility connections.
GMP
적격성평가
2026년 8월 24일
Operational Qualification (OQ) — Test Approach for Process Equipment
How OQ testing demonstrates equipment operates as intended across its specified operating range.
GMP
적격성평가
2026년 8월 24일
Performance Qualification (PQ) — Acceptance Criteria Development
How PQ acceptance criteria are derived to prove equipment performs consistently under real production conditions.
GMP
적격성평가
2026년 8월 24일
Requalification Frequency — Risk-Based Approach for Critical Equipment
How to set a risk-based requalification schedule for equipment critical to product quality.
GMP
적격성평가
2026년 8월 24일
Temperature Mapping — Qualification Approach for Cold Storage Units
How temperature mapping studies qualify cold storage units for reliable pharmaceutical storage.
GMP
적격성평가
2026년 8월 24일
Vendor Qualification — Documentation Requirements from Equipment Suppliers
What documentation should be requested from an equipment vendor to support the qualification effort.