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What is ProcEdge RIMS?

ProcEdge RIMS is a comprehensive regulatory information management solution crafted to help organizations effectively oversee the entire lifecycle of product registrations, from pre-approval documentation to post-registration compliance activities. Designed to replace inefficient spreadsheet tracking, the platform centralizes regulatory data and workflows, enabling seamless collaboration between departments and ensuring real-time data accuracy across global markets. It supports the management of multiple products across various countries, handling complex regulatory differences with a configurable data model and automated workflows. Key features include timeline tracking for submissions and renewals, query management to efficiently address regulatory authority questions, and electronic notifications to alert users about critical regulatory events. ProcEdge RIMS is compliant with international industry standards such as IDMP, GxP, GDPR, and 21 CFR Part 11, ensuring regulatory reliability and data security. The platform also provides audit trails and role-based access controls to maintain data integrity and compliance. By reducing manual data entry and eliminating redundant systems, it cuts operational costs and accelerates time to market. Its comprehensive tracking and reporting capabilities allow regulatory teams to plan submissions effectively and respond to regulatory inquiries promptly. With improved data control and visibility, companies gain a global view of product issues enabling quicker, informed decision-making. Ultimately, ProcEdge RIMS empowers regulatory professionals to meet complex compliance demands efficiently while driving faster product approvals and reducing risks.

What is EXTEDOpulse?

EXTEDOpulse provides a comprehensive RIM software suite featuring five integrated hubs that encompass every stage of pharmaceutical product development. Users have the flexibility to use the applications separately or to enhance their workflow by integrating them based on their unique requirements. The intricacies of pharmaceutical product development necessitate collaboration among multiple departments within a company, which can complicate the process. Moreover, the stringent regulations governing the industry add another layer of difficulty for life science companies with each product they seek to launch. With extensive knowledge of the life sciences sector, we promote synergy, connectivity, and innovation, ensuring that compliance is achieved without hassle. EXTEDOpulse is specifically designed to address these challenges, providing tools that facilitate connections throughout the entire lifecycle of pharmaceutical products, thus optimizing operations and boosting efficiency. In recognizing the multifaceted nature of navigating the regulated landscape of pharmaceutical products, EXTEDO strives to make this journey more manageable for its users while also promoting continuous improvement and adaptability.

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Integrations Supported

Generis CARA

Integrations Supported

Generis CARA

API Availability

Has API

API Availability

Has API

Pricing Information

$300
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Sarjen Systems Pvt Ltd

Date Founded

1998

Company Location

India

Company Website

rims.sarjen.com

Company Facts

Organization Name

EXTEDO

Date Founded

2003

Company Location

Germany

Company Website

www.extedo.com/software/overview/extedopulse

Categories and Features

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