STANDARDS MANAGEMENT SOFTWARE

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AmpleLogic: Your QC Standards Solution

AmpleLogic Standards Management Software offers comprehensive solutions for pharmaceutical QC laboratories. From primary reference standards to impurity management, our software ensures compliance, efficiency, and traceability throughout the quality control process.

Enhance Efficiency with AmpleLogic Standards Suite

AmpleLogic Standards Suite offers automated tracking, error prevention, and compliance assurance for pharmaceutical QC. With comprehensive usage logs and SOP integration, streamline your quality processes today.

Automated Quantity Management-01

Automated Quantity Management

Ensure precise tracking and inventory control.

Barcoding for Error Prevention-01

Barcoding for Error Prevention

Minimize human errors with barcode scanning.

Regulatory Compliance Assurance

Regulatory Compliance Assurance

Meet FDA and EU Annex 11 standards effortlessly.

Alerts and Reminders-01

Alerts and Reminders

Stay updated with automatic notifications and reminders.

Comprehensive Usage Logs-01

Comprehensive Usage Logs

Detailed logs for thorough tracking and auditing.

Cross-Industry Versatility-01

Cross-Industry Versatility

Suitable for various industries beyond pharmaceuticals.

Integrated SOP Adherence

Integrated SOP Adherence

Seamlessly align with existing standard operating procedures.

Streamlined Destruction Reporting

Streamlined Destruction Reporting

Simplify the process of reporting expired materials.

Tailored Solutions for Every Standard

Manage primary reference standards efficiently.

Track and validate secondary working standards accurately.

Organize and monitor standards used in laboratory analyses.

Ensure precise management and tracking of impurity standards.

Manage and trace reference solutions effectively.

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

AmpleLogic handles primary reference, working, laboratory, impurity, and reference solution standards.

Yes, AmpleLogic complies with 21 CFR Part 11, FDA regulations, and EU Annex 11.

AmpleLogic utilizes barcoding and automated quantity tracking to prevent errors.

Yes, AmpleLogic seamlessly integrates with standard operating procedures for enhanced compliance.

AmpleLogic’s software is suitable for lifesciences, food & beverages, cosmetics, medical devices and other regulated industries.

Contact us

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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