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Home » LifeSphere » Quality » Quality Document Management System

Your Single Source of Truth for Quality Content

Take greater control with purpose-built, comprehensive quality document management.

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LifeSphere® Technology is trusted by these industry leaders:
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Quality Documents

Quality Documents enables consistent and efficient compliance with support for best-in-class capabilities through the quality document management lifecycle.

Standardization

Establish common standards through pre-configured documents.

Enhanced Content Management

Manage content through the quality lifecycle, including version control and audit trails.

Global Harmonization

Harmonize document management by establishing a single asset repository accessible to cross-functional and global teams.

Deeper Insights

Gain strategic insights through impact assessment analysis.

Features

Deliver real value with Quality Documents.

Controlled Templates

Provide support for high-level policies and guidelines, through specific procedures and lower-level records.

Process Standardization

Leverage predefined workflows, metadata, versioning policies, roles, and permissions.

End-to-End Document Management

Gain support across quality assurance, quality control, manufacturing, and R&D.

Data Control

Access periodic review and document validation processes, including automatic notifications.

Global Scalability

Our solution is highly suitable for global rollouts, with a proven track record of global implementations, including support for more than 18 languages.

A Single Vendor

Establish a single, end-to-end vendor by integrating LifeSphere Reporter with your larger ecosystem, including safety, medical information, and CRM systems.

Discover NavaX

the latest automation from LifeSphere

Learn More

Discover NavaX

the latest automation 
from LifeSphere

Learn More

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Quality Document Management SystemMladen Prenc2024-12-10T09:06:36+00:00

ArisGlobal is a pivotal partner in the life sciences industry, specializing in solutions that drive drug development, safety monitoring, and regulatory compliance. We collaborate with more than 500 global life sciences companies, CROs, and government health authorities, including leading biopharmaceutical firms and regulatory bodies such as FDA, Health Canada, and NMPA.
Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.

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