OpenTextは数十年の専門知識を提供し、データのロックを解除し、人々とプロセスをつなぎ、信頼性を持ってAIを推進
企業全体でデータをシームレスに統合し、サイロを排除し、コラボレーションを改善し、リスクを軽減
AIに対応し、データを構造化され、アクセスしやすく、最適化された情報に変換
規制およびコンプライアンス要件を満たし、情報のライフサイクル全体を保護
あらゆる規模のグローバル組織に対応するスケーラブルで柔軟な導入オプションを探る
ローカルなコントロール、グローバルなスケールで信頼できるAIを活用。
コントロールとコンプライアンスを維持しながら、クラウドの価値を引き出します。
自社インフラストラクチャでデータを完全に管理
選択したクラウドでビジネス情報を保護、拡張、利用
新しい方法で情報を捉える
ビジネス、データ、目標を理解するAI
より迅速な決断が実現。安全なパーソナルAIアシスタントが作業をお手伝いします。
サプライチェーンにおける生成AIでより良い洞察を得る
AIコンテンツ管理とインテリジェントなAIコンテンツアシスタントで業務を強化
アプリの配信、開発、自動化されたソフトウェアテストの加速を実現
カスタマーサクセスのためのカスタマーコミュニケーションとカスタマーエクスペリエンスの向上
ユーザー、サービスエージェント、ITスタッフが必要な答えを見つけられるように支援
新しい方法で情報を捉える
ビジネス、データ、目標を理解するAI
より迅速な決断が実現。安全なパーソナルAIアシスタントが作業をお手伝いします。
サプライチェーンにおける生成AIでより良い洞察を得る
AIコンテンツ管理とインテリジェントなAIコンテンツアシスタントで業務を強化
アプリの配信、開発、自動化されたソフトウェアテストの加速を実現
カスタマーサクセスのためのカスタマーコミュニケーションとカスタマーエクスペリエンスの向上
ユーザー、サービスエージェント、ITスタッフが必要な答えを見つけられるように支援
一度接続するだけで、安全なB2B統合プラットフォームからすべてに連携
AI対応のコンテンツ管理ソリューションで知識を再構築
企業保護のための統合サイバーセキュリティソリューション
AIを活用したDevOpsの自動化、テスト、品質向上により、より優れたソフトウェアをより迅速に提供
忘れられないカスタマーエクスペリエンスで会話を再考
IT運用のコストと複雑さを削減するために必要な明確性を獲得
実績のあるOpenText Information Managementテクノロジーを使用したカスタムアプリケーションの構築
カスタムアプリケーションとワークフローを可能にするリアルタイムな情報フローを作成するOpenText Cloud APIを使用して、お客様独自の方法で構築
安全な情報管理と信頼できるAIの融合
データとAIの信頼を高める統合データフレームワーク
データ言語でエージェントを構築、デプロイ、反復できる場所
AIを促進するためのデータ取り込みとメタデータタグ付けを自動化するツールセット
ガバナンスを積極的かつ持続的にするためのサービスとAPIのスイート
AIのジャーニーをサポートするプロフェッショナルサービスのエキスパート
AIを活用した情報管理により、可視性が向上し、より鮮明な洞察が得られます。その方法を確認する準備はよろしいですか?
AIを活用したエンタープライズコンテンツ管理で日常業務を変革する
ITサービス管理、AIOps、可観測性のコストと複雑さを削減
サプライチェーン成功のためのAIを活用したB2B統合
コネクテッドカスタマーエクスペリエンスで価値、成長、ロイヤルティを向上
アジャイル開発とソフトウェアデリバリー?決して不可能ではありません。
エンタープライズ向けサイバーセキュリティ
AIデータ分析で洞察を引き出す
新しい方法で情報を捉える
ビジネス、データ、目標を理解するAI
より迅速な決断が実現。安全なパーソナルAIアシスタントが作業をお手伝いします。
サプライチェーンにおける生成AIでより良い洞察を得る
AIコンテンツ管理とインテリジェントなAIコンテンツアシスタントで業務を強化
アプリの配信、開発、自動化されたソフトウェアテストの加速を実現
カスタマーサクセスのためのカスタマーコミュニケーションとカスタマーエクスペリエンスの向上
ユーザー、サービスエージェント、ITスタッフが必要な答えを見つけられるように支援
認定エキスパートによるガイダンスでデジタルトランスフォーメーションを加速
認定専門家と連携して情報管理を近代化
専門家のガイダンス、マネージド サービスなどを活用してビジネス目標を達成
サポートを戦略的優位性に変える
専門的なITサービス管理で社内チームの負担を軽減
あらゆるスキルレベルのユーザーがOpenText製品を導入し、効果的に使用できるようにするためのトレーニングオプションをご紹介します。
あらゆるスキルレベルのユーザーがOpenText製品を導入し、効果的に使用できるようにするためのトレーニングオプションをご紹介します。
OpenTextは、主要なクラウドインフラストラクチャプロバイダーと提携し、OpenTextソリューションをどこでも実行できる柔軟性を提供します。
OpenTextは主要エンタープライズアプリプロバイダーと提携し、非構造化コンテンツを活用してビジネスインサイトを向上
Milestone Pharma Co. LtdDrug development and contract research organization streamlined workflows by replacing paper processes with OpenText Documentum for Life Sciences


Milestone Pharma Co. Ltd, a holding subsidiary of WuXi AppTec, was established in 2016 and is committed to becoming a world-class drug quality control platform, providing one-stop solutions for drug-quality research aimed at drug registration. Milestone Pharma has built quality-control laboratories with different technical capabilities in Nanjing and Shanghai, in compliance with global pharmaceutical law and regulations.
Because Milestone Pharma is a key link in the pharmaceutical value chain, it is crucial for the company to maintain high levels of quality in every aspect of its operations. For drug development, and contract research in particular, the company must ensure that work is properly documented, reviewed and approved by its managers and subject-matter experts.
Yinyong, quality director at Milestone Pharma, explains, “The pharmaceutical space is evolving rapidly, driven by innovations such as mRNA technology and genomic medicine. While there are many new trends on the horizon, it’s certain that quality will continue to be the foundation of our industry, and we are committed to leading the industry in quality management.”
To help its clients bring life-enhancing therapies to patients, Milestone Pharma works closely with international pharmaceutical regulators to demonstrate that new drugs are safe and effective. These and business activities such as contract research generate huge numbers of documents, all of which must be made available to regulators.
In the past, Milestone Pharma relied on paper to drive its business. However, as the company grew, the time and effort to manage rapidly increasing document volumes rose substantially, reducing operational efficiency.
“The sheer quantity of paper records flowing back and forth across the organization was beginning to slow us down,” comments Yinyong. “For example, if a client requested an urgent change to a contract research order, the relevant paper record had to be updated, reviewed and approved by one or more managers. As we lacked a clear overview of where documents were in the approval cycle, it was difficult to identify and remove bottlenecks.”
To help its clients keep their projects on track, Milestone Pharma looked for a more efficient approach to document management. The aim was to empower employees to review and approve documents more effectively while ensuring a full audit trail for regulatory compliance and audits.

Thanks to digital workflows powered by OpenText Documentum, we can now process 3.5 times more documents each month, which creates headroom for significant future business growth.
Milestone Pharma replaced paper processes with a digital solution based on OpenText™ Documentum™ for Life Sciences and OpenText™ Documentum™ for Quality and Manufacturing, enabling the company to manage thousands of documents from a single point of control.
Unify processes and seamlessly share information across the extended Life Sciences enterprise.
Control critical quality documentation, streamline and automate processes with compliance.
Milestone Pharma decided it needed to move away from paper and adopt a digital approach. The OpenText solution met the company’s core selection criteria, including the ability to enforce strict authoring standards around document taxonomies, attributes and access rights. Traceability and transparency were also crucial since Milestone Pharma would rely on document metadata to demonstrate compliance to regulators.
“During the solution evaluation process, one of the things that stood out to us was that pharmaceutical companies have been using OpenText Documentum solutions to support their businesses for over 20 years, and that gave us great confidence,” says Yinyong. “We conduct R&D and drug registration on behalf of large international enterprises, which means we must demonstrate our compliance with stringent quality standards. The OpenText solutions include templates based on global best practices—including from U.S. Food and Drug Administration and European Medicines Agency—straight out of the box.”
For Milestone Pharma, the move to paperless operations implied more than simply switching from written records to electronic documents. To build robust workflows around its digital documents, the organization turned to its trusted business partner, Tri-I Biotech Ltd.
“Tri-I Biotech are experts in delivering OpenText Documentum solutions for the pharmaceutical industry,” explains Yinyong. “Input from the Tri-I Biotech team was extremely valuable throughout the design and implementation process. For example, the team advised us on the optimal document taxonomies and helped us configure file attributes such as version numbers to track changes over the document lifecycle.”
Working with Tri-I Biotech, Milestone Pharma successfully transitioned to the new digital processes with zero disruption to day-to-day operations.
“We were extremely pleased that we were able to move from paper processes to OpenText Documentum without interrupting mission-critical activities such as research or drug registration,” adds Yinyong. “Employees across the business found it straightforward to switch to digital documents, which allowed us to start realizing the benefits almost immediately.”
For compliance purposes, OpenText Documentum offers our regulators a transparent audit trail of every change to every document, including e-signatures.
By moving to OpenText Documentum for Life Sciences and OpenText Documentum for Quality and Manufacturing, Milestone Pharma eliminated the time and costs associated with printing, mailing and filing paper.
Today, Milestone Pharma has significantly increased its document processing capacity without driving up back-office workloads. Yinyong elaborates: “Thanks to digital workflows powered by OpenText Documentum, we can now process 3.5 times more documents each month, which creates headroom for significant future business growth.”
“The solution is also making it easier for us to offer responsive services to our clients, since we’ve greatly reduced the risk of urgent approvals, such as change requests, getting lost in the shuffle. In fact, managers can even approve documents when they’re on the move, helping to avoid delays for our clients.”
By building its business on traceable digital workflows, Milestone Pharma has also reduced the time and manual effort required to prepare documentation for audits and certification processes.
“In the past, finding and retrieving paper records was a laborious and time-consuming process, but now that’s all changed,” says Yinyong. “We have a comprehensive set of attributes and metadata for each document, which makes it extremely fast and easy to find the records we need. And for compliance purposes, OpenText Documentum offers our regulators a transparent audit trail of every change to every document, including e-signatures.”
With OpenText solutions at the heart of its approach to digital document management, Milestone Pharma is in a strong position to drive growth while maintaining outstanding levels of quality across its operations.
“Our journey with OpenText Documentum for Life Sciences and OpenText Documentum for Quality and Manufacturing is just beginning, but our clients are already starting to see the benefits,” concludes Yinyong. “Working with OpenText and Tri-I Biotech, we have deployed a digital document workflow that can support the most rigorous requirements of the pharmaceutical industry, helping our clients bring life-enhancing therapies to patients faster.”Tri-I Biotech (Shanghai) Ltd is a high-tech enterprise focusing on digital empowerment construction in the life sciences industry.
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