CAPA Management Software
Drive corrective and preventive actions from quality issues through investigation, implementation, effectiveness verification, and closure.
Business Challenge
CAPA programs lose momentum without structured follow-through
Corrective and preventive actions often stall when assignments, evidence, and effectiveness checks are tracked outside the quality system.
AmpleLogic supports closed-loop CAPA management with defined workflows from initiation through effectiveness verification and approval.
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。
Quality Issue
Initiate CAPA from deviations, complaints, audits, OOS/OOT, or other quality events.
Investigation
Document investigation findings, contributing factors, and supporting evidence.
Root Cause
Record root-cause analysis outcomes reviewed by authorized personnel.
Corrective/Preventive Action
Define corrective and preventive actions with owners and due dates.
Assignment
Assign implementation tasks across functions with accountability and timelines.
Implementation
Track action completion with evidence and status updates.
Effectiveness Check
Verify whether actions addressed the issue through documented effectiveness review.
Approval
Route CAPA for quality approval after implementation and effectiveness review.
Closure
Close CAPA with retained history, linked source events, and audit trail.
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。
CAPA creation from linked quality events
Root-cause investigation documentation
Corrective and preventive action planning
Task assignment with due dates and escalations
Effectiveness check workflows separate from action closure
Multi-level review and approval
Linkage to deviations, complaints, audits, and OOS/OOT
CAPA aging and status reporting
Audit-ready CAPA history and documentation
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.
GxP & Data Integrity
Designed to support regulated quality operations
AmpleLogic provides controls that help support regulated quality processes. These capabilities alone do not guarantee regulatory compliance.
Audit Trails
Track relevant changes and activities across records, reviews, and approvals.
Electronic Signatures
Support controlled review and approval workflows with documented sign-off.
Role-Based Access
Provide access according to user responsibilities across quality processes.
Traceability
Maintain visibility across records, linked quality events, actions, and approvals.
Controlled Workflows
Standardize quality processes with configurable workflow steps and checkpoints.
Version Control
Maintain controlled versions of relevant records, forms, and supporting information.
よくある質問
よくある質問
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
カナダ（ノースヨーク、トロント）
5255 Yonge Street Suite 201, North York, ON, M2N 6P4
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。