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!

Sylogent is a life sciences partner responsible for critical data and document publishing across the organization. From protocol registration or clinical date results disclosure to medical affairs information, publication planning and resource compliance, we help ensure required work is completed - on time.

Data. Process. Software.

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PROJECTIC significantly reduces the effort to allocate budgets, plan projects and track spending across any business. The tool is ideal for heavily regulated industries with repetitive compliance-driven processes. Core projects, key dates and critical milestones are instantly visualized in the interactive timeline. This web-based tool organizes critical operations data in a flexible, yet structured method, ensuring that everyone is instantly up to date on the plan and actual progress.

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Configurable Planning Templates

Global Process Transparency

Automated Plan Updates

Milestone Matrix

Target Date Alignment

Regulation Adherence Tracking


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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.

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affordable for every budget!

Guaranteed ROI

Trusted Resource since 2002

let's talk!