OpenText는 수십 년간의 전문 지식을 통해 데이터를 활용하고, 사람과 프로세스를 연결하며, 신뢰할 수 있는 AI를 강화합니다
기업 전체의 데이터를 매끄럽게 통합하여 정보 단절을 없애고, 협업을 강화하며, 리스크를 최소화하세요
데이터를 AI가 활용 가능하고 구조화되고, 접근 가능한, 최적화된 정보로 변환하세요
규제 및 준수 요구 사항을 충족하고 정보의 수명 주기 전반에 걸쳐 보호하세요
OpenText는 사람들이 콘텐츠를 관리하고, 작업을 자동화하며, AI를 사용하고, 협업하여 생산성을 높일 수 있도록 지원합니다
전 세계 수천 개의 기업이 OpenText의 혁신적인 솔루션으로 성공을 거두고 있는 방법을 확인해 보세요
직원은 OpenText의 가장 큰 자산으로, OpenText 브랜드와 가치의 생명입니다.
OpenText가 사회적 목표를 발전시키고 긍정적인 변화를 가속화하기 위해 어떤 노력을 하고 있는지 알아보세요
디지털 혁신을 이루기 최적인 솔루션과 전문성을 갖춘 OpenText 파트너를 만나보세요
새로운 방식으로 정보 보기
비즈니스, 데이터 및 목표를 파악하는 AI
더 빠른 의사 결정을 만나보세요. 안전한 개인 AI 비서가 업무를 시작할 준비가 되었습니다.
공급망을 위한 생성형 AI로 더 나은 인사이트를 얻어보세요.
AI 콘텐츠 관리 및 지능형 AI 콘텐츠 어시스턴트를 통해 효율적으로 작업하세요.
더 빠른 앱 제공, 개발 및 자동화된 소프트웨어 테스트를 만나보세요.
고객 성공을 위해 고객 커뮤니케이션과 경험을 개선해 보세요.
사용자, 서비스 상담원 및 IT 직원이 필요한 답을 찾을 수 있도록 권한을 부여하세요.
새로운 방식으로 정보 보기
비즈니스, 데이터 및 목표를 파악하는 AI
더 빠른 의사 결정을 만나보세요. 안전한 개인 AI 비서가 업무를 시작할 준비가 되었습니다.
공급망을 위한 생성형 AI로 더 나은 인사이트를 얻어보세요.
AI 콘텐츠 관리 및 지능형 AI 콘텐츠 어시스턴트를 통해 효율적으로 작업하세요.
더 빠른 앱 제공, 개발 및 자동화된 소프트웨어 테스트를 만나보세요.
고객 성공을 위해 고객 커뮤니케이션과 경험을 개선해 보세요.
사용자, 서비스 상담원 및 IT 직원이 필요한 답을 찾을 수 있도록 권한을 부여하세요.
한 번만 연결하면 안전한 B2B 통합 플랫폼으로 모든 대상과 연결할 수 있습니다.
AI가 활용 가능한 콘텐츠 관리 솔루션으로 지식 재구성
기업 보호를 위한 통합 사이버 보안 솔루션
AI 기반 DevOps 자동화, 테스트 및 품질을 통해 더 나은 소프트웨어를 더 빠르게 제공
잊을 수 없는 고객 경험으로 대화 재창조
IT 운영의 비용과 복잡성을 줄이기 위해 필요한 명확성 확보
검증된 OpenText 정보 관리 기술을 사용하여 맞춤형 애플리케이션 구축
사용자 정의 애플리케이션 및 워크플로를 지원하는 실시간 정보 흐름을 제공하는 OpenText Cloud API를 사용하여 원하는 방식으로 구축
안전한 정보 관리가 신뢰할 수 있는 AI를 만나다
데이터와 AI의 신뢰를 높이는 통합 데이터 프레임워크
데이터 언어로 에이전트를 구축, 배포 및 반복할 수 있는 공간
AI를 강화하기 위해 데이터 수집 및 메타데이터 태그 지정 자동화를 지원하는 도구 세트
거버넌스를 사전 예방적이고 지속 가능하게 만드는 서비스 및 API 제품군
AI 여정을 도와주는 전문 서비스 전문가
새로운 방식으로 정보 보기
비즈니스, 데이터 및 목표를 파악하는 AI
더 빠른 의사 결정을 만나보세요. 안전한 개인 AI 비서가 업무를 시작할 준비가 되었습니다.
공급망을 위한 생성형 AI로 더 나은 인사이트를 얻어보세요.
AI 콘텐츠 관리 및 지능형 AI 콘텐츠 어시스턴트를 통해 효율적으로 작업하세요.
더 빠른 앱 제공, 개발 및 자동화된 소프트웨어 테스트를 만나보세요.
고객 성공을 위해 고객 커뮤니케이션과 경험을 개선해 보세요.
사용자, 서비스 상담원 및 IT 직원이 필요한 답을 찾을 수 있도록 권한을 부여하세요.
OpenText는 주요 클라우드 인프라 제공업체와 협력하여 어디서나 OpenText 솔루션을 실행할 수 있는 유연성을 제공합니다
OpenText는 최고의 엔터프라이즈 앱 제공업체와 협력하여 비정형 데이터를 활용함으로써 더 나은 비즈니스 인사이트를 제공합니다
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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