More Regulations, Fewer Resources, Less Time

The FDA, EMA and other international regulators are aggressively pushing for timely clinical trial protocol registration and clinical data disclosure. Manual, decentralized processes are expensive, inefficient and create a compliance risk as shortened timelines are almost impossible to satisfy.

We can help!

Data is lifeblood of every organization. It is the foundation of every decision, activity and action. Now more than ever it is critical that companies utilize data to maximize compliance, productivity and strategy. We realize that structured information management is a significant change for the pharmaceutical industry, so we must work with many stakeholders across the organization to ensure success. That is why we offer more that just software, but provide data and process services to maximize enterprise value.

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software

SYQUENCE is a flexible web-based tool that helps companies organize, centralize and standardize critical data in a secure database. Experts agree it is not recommended that business critical data be managed in desktop products like Excel, Word, PowerPoint and Outlook. These products decrease transparency, data security and compliance adherence while increasing risk management liabilities.

Please contact us today if you are interested in learning more about how SYQUENCE can help your organization stay compliant, achieve submission timelines and maximize data consistency.

Controlled Data Lists

Master Data Sets

Controlled Vocabulary

Integrated Structured Templates

Data Sharing Templates

Automated Task Creation

Information Workflow

Dynamic Structured Publishing

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we'll do it for you!

Enterprise Perspective

We understand the overall issues across your company.

Business Expertise

We work with all of the business units today.

Operational Innovation

We can help you transform your company - with minimal disruption.

software

affordable for every budget!

Guaranteed ROI

Trusted Resource since 2002

let's talk!