표준
약전 및 국제표준(USP/EP/ICH/ISO/WHO).
표준
2026년 8월 25일
21 CFR Part 210/211 — US GMP Regulation Structure Overview
How 21 CFR Parts 210 and 211 are organized and what each subpart addresses.
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표준
2026년 8월 25일
EU GMP Annex 1 — 2022 Revision Key Changes for Sterile Manufacturing
The most significant changes introduced by the 2022 revision of EU GMP Annex 1.
표준
2026년 8월 25일
ICH Guidelines — Overview of Quality (Q), Safety (S), Efficacy (E) Series
A map of the ICH Q/S/E guideline series and how they fit together across the product lifecycle.
표준
2026년 8월 25일
ISO 13485 — Quality Management for Medical Devices Overview
What ISO 13485 requires of a medical device quality management system.
표준
2026년 8월 25일
ISO 14644 — Cleanroom Classification Standard Overview
What the ISO 14644 series covers beyond classification, including monitoring and testing.
표준
2026년 8월 25일
ISO 15378 — Primary Packaging Materials Quality Management
What ISO 15378 adds on top of ISO 9001 for primary packaging material manufacturers.
표준
2026년 8월 25일
ISO 9001 — Quality Management System Requirements for Pharma Suppliers
What ISO 9001 certification means for a pharmaceutical supply chain vendor, and its limits.
표준
2026년 8월 25일
Pharmacopeial Harmonization — USP/EP/JP Convergence Status
How the USP-EP-JP harmonization process works and where meaningful differences still remain.
표준
2026년 8월 25일
USP-NF — Structure and How to Navigate Monographs
How the USP-NF is organized and how to read a monograph to find the requirements that matter.
표준
2026년 8월 25일
WHO GMP Guidelines — Comparison with EU/FDA GMP Requirements
Where WHO GMP guidance aligns with, and differs from, EU and FDA GMP expectations.
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