eQMS/Core Quality Actions/CAPA管理
医薬品CAPA管理ソフトウェア

CAPA管理

Drive closed-loop corrective and preventive actions from initiation through effectiveness verification — with AI-powered effectiveness intelligence that automatically compares new CAPAs against open effectiveness checks of similar nature, AI-assisted root cause analysis, automated task tracking, and audit-ready documentation.

40%

Faster CAPA Closure

100%

Source-to-Closure Tracing

AI

Effectiveness Intelligence

Zero

Missed Effectiveness Checks

エンドツーエンドのプロセスフロー

仕組み

開始からクローズまでの体系的なワークフロー。すべての段階に組み込まれたコンプライアンスチェックポイントと規制上の正当性を備えています。

1

CAPA Initiation

Auto-initiate CAPA from deviations, complaints, audit findings, or OOS events with pre-linked source records and AI-powered duplicate detection against existing open CAPAs.

2

Root Cause Analysis

AI-assisted RCA with pattern matching from historical data, guided investigation tools, and evidence collection.

3

Action Planning

Build corrective and preventive action plans with task assignments, risk priority, due dates, and evidence requirements.

4

Implementation

Execute actions with milestone tracking, evidence capture, and automatic updates to linked quality records.

5

AI Effectiveness Intelligence

AI continuously monitors open effectiveness-check CAPAs and automatically compares every incoming CAPA of similar nature — flagging overlaps, recommending consolidation, and preventing redundant investigations.

6

Closure & Archive

Final approval with completeness validation, regulatory-ready documentation, and archival for inspection readiness.

機能・能力

主要機能

ライフサイエンスの規制要件と業務卓越性のために設計された包括的な機能。

01

Auto-initiation of CAPA from linked deviations, complaints, audit findings, and OOS events — a unified quality event CAPA management system

02

AI-powered root cause analysis software for pharma CAPA investigations, with pattern matching from historical CAPA data to prevent recurring deviations

03

CAPA workflow automation with configurable task assignments, due dates, risk priority, and evidence requirements — replacing manual CAPA tracking and spreadsheet-based CAPA management

04

Parallel corrective and preventive action tracking with separate owners, timelines, and CAPA documentation management for full regulatory defensibility

05

Built-in CAPA effectiveness check software with predefined success criteria, re-testing protocols, and automated CAPA closure and effectiveness tracking

06

AI-powered effectiveness intelligence — automatically compares every new CAPA against open effectiveness-check CAPAs of similar nature, flags potential duplicates, and recommends consolidation or cross-referencing to prevent redundant investigations

07

Extension management with documented justification, multi-level approval chains, and complete audit trail for GxP compliant CAPA processes

08

Real-time dashboards showing CAPA aging, overdue actions, CAPA effectiveness tracking, and recurring deviation management insights across all sites

40% faster CAPA closure with automated CAPA workflow software
100% traceability from source quality event to final CAPA closure
AI-driven effectiveness intelligence eliminates redundant CAPA investigations

実際の活用事例

ユースケース

ライフサイエンスオペレーション全体で測定可能な価値を提供するモジュールの実証済みシナリオ。

Recurring Deviation Pattern

Identify recurring deviations, group them into a systemic CAPA, conduct comprehensive root cause analysis, and implement preventive measures.

Audit Finding Remediation

Convert critical and major audit findings into tracked CAPAs with defined timelines, responsible parties, and effectiveness verification.

AI-Driven Effectiveness Overlap Detection

When a new CAPA is created, AI automatically scans all open effectiveness-check CAPAs of similar nature — flagging potential duplicates, recommending cross-references, and surfacing existing corrective actions that may already address the same root cause.

Regulatory Inspection Response

Rapidly create and track CAPAs in response to regulatory observations with documented evidence and timeline compliance.

よくある質問

よくある質問

CAPA管理の近代化を始めませんか?

AmpleLogic eQMSが個別デモを通じてどのようにCAPA管理ワークフローを変革できるかをご確認ください。

私たちの グローバル オフィス

必要な場所に、私たちがいます。グローバルにつながる、ローカルに届ける。

インド

Melange Tower, 2nd Floor, Wing-C, Patrika Nagar, HITEC City, Madhapur, Hyderabad - 500081, Telangana, India

アメリカ合衆国(ダラス)

17330 Preston Road Suite 200D, Dallas, TX, 75252

カナダ(ノースヨーク、トロント)

5255 Yonge Street Suite 201, North York, ON, M2N 6P4

オーストラリア(メルボルン)

Level 14, 330 Collins Street, Melbourne, VIC, 3000

韓国(大邱)

Daegu Trade Centre, 8/F. 489, Dongdaegu-ro, Daegu, 41256

アイルランド(ダブリン)

Block 1, Blanchardstown Corporate Park Ballycoolen Road, Dublin, D15 AKK1

シンガポール

1 Scotts Road, #24-10 Shaw Centre, Singapore, Singapore, 228208

ライフサイエンスの最前線へ

最新の製品アップデート、コンプライアンスニュース、業界インサイトをお届けします。