BRIMS Software

Efficiently Manage Batch Records, Ensure Compliance

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AmpleLogic BRIMS: Streamlining Batch Record Management

AmpleLogic BRIMS is a robust software solution designed to streamline and automate batch record management processes in pharmaceutical, biotech, and life sciences industries. With compliance to regulatory standards such as 21 CFR Part 11, cGMP, GMP, MHRA, EU Annex 11, and more, BRIMS ensures adherence to stringent industry regulations.

It offers features like automated batch issuance, controlled printing, customizable reporting, and integrated workflow automation, simplifying document management tasks. BRIMS enhances efficiency, reduces errors, and improves quality assurance, ultimately leading to enhanced client satisfaction and minimized compliance risks.

Efficiency Elevated: BRIMS Features

Streamlined Batch Record Management-01

Streamlined Batch Record Management

Automated batch issuance, document versioning, and audit trail functionalities.

Controlled Printing and Access-01

Controlled Printing and Access

Privileged access constraints for controlled printing and secure document management.

Customizable Reporting

Customizable Reporting

Flexible report generation tailored to specific requirements.

Integrated Workflow Automation

Integrated Workflow Automation

Predefined workflows for initiation, authorization, and destruction processes.

Elevate Efficiency with BRIMS

Adhere to regulatory standards and minimize compliance risks.

Speed up processes and reduce errors for improved productivity.

Maintain high-quality standards and enhance client satisfaction.

Optimize resources and decrease time-to-market with streamlined processes.

Hear From Our Customers

Paramita-Sarkar
Paramita Sarkar Vice President, OCuSOFT

AmpleLogic understood the limitations we had as a growing organization. With the budget constraints we had, we couldn’t have been able to find a better, flexible and customizable partner than AmpleLogic. We appreciate the team.
Om-Prakash-Sule
OM Prakash Sule Vice President, Windlas

Windlas Biotech is committed for transparent Quality Management System and other records. "This is the reason we opted for part 11 compliant partner AmpleLogic. Great contribution by AmpleLogic team to make it Live in shortest possible time"
Georges-Ibrahim
Georges Ibrahim CQO, Julphar

AmpleLogic’s QMS application has higher level of transparency and efficacy. It has helped us in tracking day to day quality processes to manage huge information and data and also have transparency in managing
complaints.

Frequently Asked Questions

BRIMS complies with 21 CFR Part 11, cGMP, GMP, MHRA, EU Annex 11, and other regulatory standards.

BRIMS manages document versioning, ensuring the latest versions are available and archived appropriately.

Yes, BRIMS integrates with other systems like Formulations and APIs for seamless workflow management.

BRIMS provides controlled printing and access with privileged access constraints, ensuring document security.

BRIMS maximizes compliance, enhances efficiency, improves quality, and reduces errors, leading to client satisfaction and regulatory adherence.

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Your Pharma Automation Starts Here

We’re here to address your inquiries and assist you in identifying the solutions that best align with your requirements. Here’s why choosing us is your strategic advantage:

Your benefits:
  • Client-oriented
  • Independent
  • Competent
  • Results-driven
  • Problem-solving
  • Transparent
What happens next?
1

Schedule a call at your convenience 

2

Discovery and consultation session 

3

Get your custom proposal 

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