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📁 Pharmacovigilance
📋 Adverse Event Reporting
🔧 TARA PV

TARA PV

An all-encompassing, online pharmacovigilance safety database.

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Overview

TARA PV is an online pharmacovigilance safety database designed for processing, storing, analyzing, and reporting adverse events for pharmaceuticals, medical devices, and vaccines. Developed by MedGenesis Ltd, an ISO 9001 and ISO 27001 accredited software firm, TARA PV offers a user-friendly interface and full compliance with regulations such as 21 CFR Part 11, GxP, and ICH standards.

✨ Key Features

  • Online safety database
  • User-friendly interface
  • Compliance with 21 CFR Part 11, GxP, and ICH standards
  • Support for pharmaceuticals, medical devices, and vaccines

🎯 Key Differentiators

  • Focus on user-friendliness and simplicity
  • Strong compliance credentials (ISO 9001 and ISO 27001)
  • Developed by a specialized software firm with a focus on quality

Unique Value: Offers a user-friendly, compliant, and secure online pharmacovigilance database from an ISO-certified developer.

🎯 Use Cases (3)

Adverse event management for small to medium-sized life sciences companies Organizations seeking a simple and compliant PV database Safety reporting for medical devices and vaccines

✅ Best For

  • Full adherence to 21 CFR Part 11, GxP, and ICH standards.

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Large enterprises with complex, global pharmacovigilance needs.

🏆 Alternatives

SafetyEasy DrugCard Other SMB-focused PV databases

Provides a higher level of certified quality and security (ISO 27001) compared to some other solutions in its market segment.

💻 Platforms

Web

🛟 Support Options

  • ✓ Email Support
  • ✓ Phone Support
  • ✓ Dedicated Support (Enterprise tier)

🔒 Compliance & Security

✓ HIPAA ✓ BAA Available ✓ GDPR ✓ ISO 27001 ✓ 21 CFR Part 11 ✓ GxP ✓ ICH standards ✓ ISO 9001

💰 Pricing

Contact for pricing

Free tier: NA

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