--- description: Qualcy QMSを実際に使用したユーザーのレビューから、製品の機能や価格、メリットデメリットをご覧いただけます。類似製品との比較も簡単、ぴったりのSaaSが見つかるはず！ image: https://gdm-localsites-assets-gfprod.imgix.net/images/capterra/og_logo-e5a8c001ed0bd1bb922639230fcea71a.png?auto=format%2Cenhance%2Ccompress title: Qualcy QMSとは？ | 機能や料金、導入事例をご紹介【キャプテラ】 --- 現在地表示: [ホーム](/) > [QMS（品質管理システム）](/directory/30099/quality-management/software) > [Qualcy QMS](/software/182641/document-management-system) # Qualcy QMS Canonical: https://www.capterra.jp/software/182641/document-management-system ページ：1 / 2\ 次へ: [次ページ](https://www.capterra.jp/software/182641/document-management-system?page=2) > Qualcy Bio-Med QMS Softwareは、中小規模のバイオテクノロジー、製薬および医療機器企業によるQMS記録管理を簡素化します。 > > 評価：22人のユーザーによる評価は**5.0/5**。**おすすめ度**で最高の評価。 ----- ## 概要 ### Qualcy QMSの対象ユーザー 医療機器、製薬、バイオテクノロジー企業。 ## 簡単な統計と評価 | 測定基準 | 評価 | 詳細 | | **総合評価** | **5.0/5** | 22 レビュー | | 使いやすさ | 4.7/5 | レビュー全体に基づく | | カスタマー・サポート | 4.9/5 | レビュー全体に基づく | | 価格の妥当性 | 4.9/5 | レビュー全体に基づく | | 機能 | 4.6/5 | レビュー全体に基づく | | おすすめ率 | 100% | (10/10 おすすめ度) | ## 企業情報 - **キャプテラについて**: Qualcy Systems - **ロケーション**: San Deigo, アメリカ - **設立**: 2014 ## ビジネスコンテキスト - **価格プラン**: $99.00 - **価格モデル**: (無料版が利用可能) (無料のトライアル) - **対象となる企業**: 2～10, 11～50, 51～200, 201～500, 501～1,000, 1,001～5,000, 5,001～10,000, 10,000+ - **デプロイとプラットフォーム**: クラウド、SaaS、ウェブベース, Mac（デスクトップ）, Windows（デスクトップ）, Windows（オンプレミス）, Linux（オンプレミス）, Android（モバイル）, iPhone（モバイル）, iPad（モバイル） - **サポートされる言語**: 英語 - **利用可能な国**: アイスランド, アイルランド, アゼルバイジャン, アフガニスタン, アメリカ合衆国, アラブ首長国連邦, アルジェリア, アルゼンチン, アルバ, アルバニア, アルメニア, アンギラ, アンゴラ, アンティグア・バーブーダ, アンドラ, イエメン, イギリス, イスラエル, イタリア, イラク さらに199件 ## 機能 - Asset Lifecycle Management - アクセス制御・許可 - アラート／通知 - インシデント管理 - クレーム管理 - コンプライアンス管理 - タスク管理 - ダッシュボード - トレーニング管理 - ドキュメントのコーディングおよび制御 - フォーム管理 - メンテナンスのスケジューリング - メンテナンス管理 - モバイル・アクセス - リスク・マネジメント - リスク評価 - レポートと統計 - レポート／分析 - 不適合追跡 - 予防メンテナンス - 作業発注管理 - 品質管理 - 在庫管理 - 変更管理 - 技術者管理 - 是正措置・予防措置 (CAPA) - 楽器管理 - 機器管理 - 点検管理 - 監査管理 - 監査計画 - 監査証跡 - 証明書印刷、ラベル印刷 - 資産追跡 - 較正スケジューリング - 較正管理 ## サポートのオプション - メール/ヘルプデスク - 電話サポート - チャット対応有 ## Category - [QMS（品質管理システム）](https://www.capterra.jp/directory/30099/quality-management/software) ## 関連カテゴリー - [QMS（品質管理システム）](https://www.capterra.jp/directory/30099/quality-management/software) - [校正管理システム](https://www.capterra.jp/directory/30214/calibration-management/software) - [設備保全管理システム (CMMS)](https://www.capterra.jp/directory/30032/cmms/software) - [監査ツール](https://www.capterra.jp/directory/30664/audit/software) - [CAPAシステム](https://www.capterra.jp/directory/31343/corrective-and-preventive-action/software) ## 代替製品 1. [QT9 QMS](https://www.capterra.jp/software/97557/qt9-quality-management) — 4.8/5 (118 reviews) 2. [MasterControl Quality Excellence](https://www.capterra.jp/software/148577/mastercontrol) — 4.5/5 (534 reviews) 3. [SafetyCulture](https://www.capterra.jp/software/141080/iauditor) — 4.6/5 (353 reviews) 4. [Qualio](https://www.capterra.jp/software/134050/quality-management-software) — 4.5/5 (129 reviews) 5. [Dot Compliance](https://www.capterra.jp/software/192574/dot-compliance) — 4.4/5 (87 reviews) ## レビュー ### "Impressive Asset Management System" — 5.0/5 > **Jaimin** | *2026年4月23日* | 医療機器 | おすすめ評価：10.0/10 > > **良いポイント**: What I liked most about Qualcy QMS is how seamlessly it brings all quality processes into one unified, easy-to-use platform. The interface is clean and intuitive, which makes it simple for teams to adopt without extensive training—something that’s especially valuable in a regulated pharma environment. > > **改善点**: I also appreciated how efficient it made audit preparation. During inspections, information can be retrieved quickly, with clear traceability and well-organized documentation. This not only saves time but also leaves a strong impression on auditors, demonstrating a high level of control and maturity in the quality system. > > We recently implemented an Asset Management System for our pharmaceutical operations, and it has exceeded expectations in every way. The platform is intuitive, highly configurable, and aligns seamlessly with GMP requirements, making it easy to manage equipment lifecycle, calibration schedules, maintenance activities, and documentation in a fully compliant manner. The audit trail functionality and data integrity controls are especially robust, giving us confidence in meeting regulatory expectations. What truly stood out was how impressive the system proved to be during our most recent FDA audit. The auditor specifically noted the system’s organization, traceability, and ease of access to critical records. For a small pharma company, having such a reliable and well-structured system significantly enhanced our ability to present data quickly and accurately, which contributed to a smooth and successful audit experience. Overall, this Asset Management System has been a game-changer for our operations—streamlining processes, improving compliance, and strengthening our audit readiness. Highly recommended for any pharmaceutical company looking to elevate their quality and asset management practices. ----- ### "Qualcy is a good choice" — 5.0/5 > **Brian** | *2025年6月5日* | 医療機器 | おすすめ評価：10.0/10 > > **良いポイント**: We really like the ability to do traceability between requirements docs within the eQMS. And the system is very comprehensive. > > **改善点**: In many environments, the day to day reality of "doing quality" can be challenging. It's more of a behind the scenes function, unlike more "glossy" departments like sales, engineering or executive management. Having integration with traceability forces the quality function to interact with engineering functions more frequently, which is good for efficiency, but some engineering personalities can be challenging. > > The service is fantastic. Our POC is very responsive, knowledgeable and patient. Their attention to detail and effective training make our eQMS efforts both enjoyable and successful. ----- ### "Qualcy eQMS" — 4.0/5 > **Carl** | *2022年11月4日* | 医療機器 | おすすめ評価：9.0/10 > > **良いポイント**: Document Control is easy to implement and easy to use. Very intuitive with a Draft Cabinet, Release Cabinet, Change Control etc. > > **改善点**: We are working on the Risk Management to comply with 14971. Also templates took a little longer to learn and implement for requirements. More templates also need to be added for forms. > > The software was easy to set up, easy to use, and the support is readily available when needed. We are working through a few issues, but no deal breakers and I would recommend this software to other medical device companies as long as the risk management is updated for compliance. ----- ### "Great QMS System for a fair price" — 5.0/5 > **Hari** | *2026年2月5日* | 薬品 | おすすめ評価：10.0/10 > > **良いポイント**: Qualcy QMS provides a centralized, compliant platform for managing quality and operational processes including asset management, CAPA, document control, training, audits, and change management. > > **改善点**: Workflow setup requires planning.Template formatting rules need to be learned.Needs structured rollout. > > Overall, the experience with Qualcy QMS has been positive, particularly in environments requiring structured quality management and regulatory compliance. The platform provides a centralized system for managing quality processes, documentation, and asset lifecycle activities, which improves traceability, audit readiness, and process consistency. ----- ### "Qualcy is an economical choice for quality management" — 5.0/5 > **Akshaya** | *2025年5月29日* | 健康、ウェルネス、フィットネス | おすすめ評価：9.0/10 > > **良いポイント**: Qualcy is affordable eQMS option, has good customer service, and provides the functionality I need in an eQMS. > > **改善点**: The user interface of the eQMS could use some updates to make it easier/more intuitive. Sometimes the server is down, but this is usually resolved in a few hours. > > Good experience, it's an affordable option for my startup and gets the job done. Exactly what I need. ----- ページ：1 / 2\ 次へ: [次ページ](https://www.capterra.jp/software/182641/document-management-system?page=2) ## リンク - [Capterraで表示する](https://www.capterra.jp/software/182641/document-management-system) ## このページは以下の言語で利用できます | ロケール | URL | | de | | | de-AT | | | de-CH | | | en | | | en-AE | | | en-AU | | | en-CA | | | en-GB | | | en-IE | | | en-IL | | | en-IN | | | en-NZ | | | en-SG | | | en-ZA | | | es | | | es-AR | | | es-CL | | | es-CO | | | es-CR | | | es-DO | | | es-EC | | | es-MX | | | es-PA | | | es-PE | | | fr | | | fr-BE | | | fr-CA | | | fr-LU | | | it | | | ja | | | ko | | | nl | | | nl-BE | | | pl | | | pt | | | pt-PT | | | sv | | | tr | | ----- ## 構造化データ