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AmpleLogic

Low Code No Code Platform for Pharma.

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Overview

AmpleLogic offers a range of software solutions for the pharmaceutical industry, built on a low-code platform. Their CAPA Management software helps pharma and biotech companies manage the entire CAPA lifecycle, ensuring compliance with standards like FDA 21 CFR Part 11, ISO 13485, and GMP guidelines.

✨ Key Features

  • CAPA Management
  • Change Control
  • Deviation Management
  • Audit Management
  • Document Management
  • Training Management (LMS)

🎯 Key Differentiators

  • Built on a low-code/no-code platform for faster deployment and customization
  • Specific focus on the pharmaceutical industry
  • Modular approach to QMS

Unique Value: Provides a highly configurable suite of QMS solutions on a low-code platform, enabling pharmaceutical companies to efficiently manage compliance and quality processes.

🎯 Use Cases (3)

Managing the CAPA lifecycle from initiation to resolution Ensuring compliance with FDA, ISO, and GMP requirements Integrating CAPA activities with other quality systems like audits and deviations

✅ Best For

  • Empowers pharmaceutical and biotech industries to manage CAPA lifecycles and meet regulatory standards.

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • May not be suitable for non-pharmaceutical industries.

🏆 Alternatives

MasterControl Veeva Systems ComplianceQuest

The low-code platform allows for greater flexibility and faster customization compared to traditional, hard-coded QMS systems.

💻 Platforms

Web

🔌 Integrations

Other QMS modules (OOS, OOT, Change Control, etc.)

🛟 Support Options

  • ✓ Email Support
  • ✓ Live Chat
  • ✓ Phone Support
  • ✓ Dedicated Support (Varies tier)

🔒 Compliance & Security

✓ GDPR ✓ SSO ✓ FDA 21 CFR Part 11 ✓ EU Annex 11 ✓ GMP ✓ ISO 13485

💰 Pricing

Contact for pricing
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