LIFESPHERE® 

Publishing

Delivering Simplicity to the Entire Regulatory Submissions Publishing Process.

A simple yet powerful submissions management application.

LifeSphere Publishing is a simple yet powerful submissions management application that enables life science organizations to easily compile, publish, and validate regulatory submissions with full support for all major global eCTD requirements.

BENEFITS
LifeSphere Clinical

End-to-End Publishing in One Application

LifeSphere Publishing provides an all-in-one, pre-validated cloud application for dossier planning and assembly, and publishing of regulatory submissions, giving regulatory teams the power to accomplish more in a single application. Modern cloud architecture delivers free and seamless upgrades, ensuring a future-proof application that’s always up to date with the latest regulatory requirements.

Streamline Submissions

Built to make the publishing process more efficient, LifeSphere Publishing uses native workflow automation to proactively navigate users through assigned activities, while hyperlinking and bookmarking capabilities deliver even greater time savings to users. LifeSphere Publishing was also created with the end-user in mind, featuring an intuitive, easy-to-navigate interface that enhances the experience of compiling, publishing, and validating submissions.

LifeSphere Clinical

Unify Regulatory

LifeSphere Publishing is part of the unified, end-to-end LifeSphere Regulatory platform, connecting with LifeSphere RIMS and LifeSphere EasyDocs out-of-the-box to provide a seamless experience across regulatory information, document and dossier management. With this unified platform approach, teams gain a single source of truth for data and documents, with significant efficiency and quality improvements.

FACT SHEET
Delivering simplicity to the entire regulatory submissions publishing process

LifeSphere Publishing is a simple yet powerful submissions management application that enables life science organizations to easily compile, publish, and validate regulatory submissions with full support for all major global eCTD requirements.

WEBINAR

Regulatory Affairs Transformation Drivers for Small and Medium Life Sciences Companies

WHITE PAPER
Regulatory 2025: Developing an Effective 10-Year Strategy for Technology-Enabled Regulatory Transformation

To achieve an objective of regulatory 2025 and beyond, companies will need to harmonize processes and implement a central technology platform. They will need to establish a platform from which the rest of the organization can consolidate data and proactively measure metrics internally.

BLOG
 ArisGlobal Insights – Interview with Pratyusha Pallavi

This is the third in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal. Senior Director, Regulatory Product Head at ArisGlobal, Pratyusha Pallavi, spoke of her role, the department vision, and product implementation.

FEATURES

Improve Efficiency, Productivity, and Cost Savings.

eCTD Submission Lifecycle Support

Manage the submission lifecycle, with full support for all major global eCTD requirements, including FDA applications and submissions.

Hyperlinking and Bookmarking

Create hyperlinks and bookmarks to streamline the submission process.

Workflow Automation

Workflow automation proactively navigates users through assigned activities

Real-Time Insights

An easily accessible real-time dashboard gives companies full visibility into submissions and related document status.

Pre-Validated Solution

Pre-validated deployment on the AWS cloud eliminates internal infrastructure and the need for costly upgrades.

Easy Connectivity

Built on an open architecture to enable seamless API connections with existing IT environments.

Easy Integration

Connects with existing systems via open architecture, leveraging API connectors and web services.

Worry-Free Implementation

Fast, professional implementation teams adhere to industry best practices to get your teams up and running quickly.

RESULTS

Delivering Real Results to a Global Client Base

80

%

Of Top 50 Biopharmas

80% of the top 50 biopharma companies are our clients

30

years

Leader in Life Sciences

Building software to streamline life sciences innovation

100

%

Compliance

100% compliance with all present and upcoming regulatory standards

PARTNERS

Partnering With the Industry’s Best

Contact Us

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