Top 10 ORA IMO Alternatives & Competitors

Top 10 Alternatives to ORA IMO Recently Reviewed By G2 Community

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MasterControl Quality Management System
By MasterControl
4.3/5
(498)
Product Description
MasterControl Inc. produces QMS software solutions which enable regulated companies to get their products to market faster, while reducing overall costs and increasing internal efficiency. MasterControl securely manages a company's critical information throughout the entire product lifecycle.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

Clinical Research Suite
By ResearchManager
3.8/5
(205)
Product Description
Research Manager supports researchers and organisations in preparing, executing and administering (clinical) research data. Our expertise is the collection, validation and enrichment of data. With Research Manager, we offer a research platform that allows researchers to have all functionalities and information in one place and to share it with each other. The platform facilitates researchers who want to be prepared for a future where the patient, access to data, and sharing data are key.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

Kivo
By Kivo
5/5
(17)
Product Description
Kivo makes simple and affordable document management systems including RIM, eTMF, and QMS. A single license grants access to all our solutions, so you can supercharge cross-functional collaboration without breaking the bank. Fully validated, Part 11 and SOC 2 compliant, Kivo is designed forGxP.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems
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Veeva Vault RIM
By Veeva
4.6/5
(10)
Product Description
The Vault RIM Suite provides fully integrated regulatory information management (RIM) capabilities on a single cloud-based platform including submission document management, product registration management, health authority correspondence and commitments, submission archiving, and comes with fully integrated IDMP capabilities.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

RegDesk
By RegDesk
4.9/5
(7)
Product Description
RegDesk is the next generation RIMS software with AI technology built exclusively for medical device and diagnostic companies. It is a one stop solution for regulatory teams.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

AmpleLogic Regulatory Information Management System (RIMS)
By AmpleLogic
5/5
(2)
Product Description
RIMS (Regulatory Information Management System) allows companies to team up, preserve application information data from various locations and enhance the processes of preparing a submission, as well as simplify the publishing and tracking of all regulatory activities that support a product’s complete life cycle.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

Essenvia
By Essenvia
4.5/5
(2)
Product Description
Essenvia is a MedTech RIM Platform to manage regulatory workflows across the total product lifecycle, accelerate global market access, and generate exponential business value. The Platform makes the lives of MedTech Regulatory Teams easier by supporting Global Registrations, Submissions, Change Assessment, and Regulatory Intelligence.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

Validfor VLM
By Validfor
5/5
(2)
Product Description
Validfor is a digital validation lifecycle management platform that modernizes how regulated organizations manage their computerized system validations. Designed for the life sciences, pharmaceutical, and medical device industries, Validfor centralizes all validation activities in one secure and compliant environment. By replacing traditional manual validation with a digital, data-driven approach, Validfor enables teams to plan, execute, and track validation processes with real-time visibility and accuracy. The platform includes built-in templates, electronic approvals, and full traceability to ensure regulatory compliance and consistent documentation quality. Whether you’re managing a single system or an enterprise-wide validation program, Validfor helps your organization stay audit-ready, improve collaboration, and maintain complete data integrity while saving time and reducing compliance risk.
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

PvEdge
By Sarjen System
5/5
(1)
Product Description
This is a trusted industry-ready, cloud-based Pharmacovigilance and Safety Database software. It is pre-validated and is quick to implement, providing faster ROI with the added benefit of data migration. What PvEdge offers: 1. Manage Drug, Device, Vaccines & Combinational Products' Core Case Processing with ICSR Gateway Submission 2. Product Inquiry (MICC Tool) 3. Literature Surveillance 4. Triage Management 5. Specialised for Human & Veterinary Vigilance 6. Safety Data Exchange Agreement System (SDEAs) 7. Pharmacovigilance Quality Management 8. eCTD Publishing - PADER/ PSUR
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Categories in common with ORA IMO:
Regulatory Information Management (RIM) Systems

G2 Deals

Buying software just got smarter. And cheaper.

This is how G2 Deals can help you:

• Easily shop for curated – and trusted – software
• Own your own software buying journey
• Discover exclusive deals on software

See Exclusive Offers