Veeva Systems

Veeva Systems Inc
★★★★★ 4.1 / 5
19 reviews

Veeva Systems provides the industry cloud for life sciences, offering solutions for clinical operations, data management, and regulatory compliance to enhance efficiency and inspection readiness.

Veeva Systems is a leading provider of the industry cloud tailored for life sciences organizations. Their comprehensive suite of solutions addresses critical aspects of clinical research, regulatory affairs, and quality management. Specializing in areas such as clinical operations, data management, and inspection readiness, Veeva offers products like Veeva eTMF, Veeva CTMS, and Veeva Payments. These tools are designed to streamline trial processes, automate training, centralize disclosures, and improve site engagement, ultimately helping companies achieve greater efficiency and maintain compliance. With a focus on innovation and collaboration, Veeva empowers industry leaders to navigate complex challenges, from accelerating site activation with Veeva Study Startup to ensuring end-to-end trial management. Their commitment to advancing the life sciences sector is evident in their continuous development of integrated platforms that support a better future for healthcare.

About

**Who they are**
Veeva Systems provides the industry cloud for life sciences, offering solutions designed to enhance efficiency and inspection readiness. They focus on cloud-based software for clinical operations, data management, and regulatory compliance.

**Expertise & scope**
* Veeva Development Cloud
* Veeva Clinical Platform
* Clinical Operations solutions
* Veeva eTMF for inspection readiness
* Veeva CTMS for end-to-end trial management
* Veeva Payments for faster site payments
* Veeva Study Startup to accelerate site activation
* Veeva RTSM for randomization and supply management
* Veeva Site Connect for automated information sharing
* Veeva Study Training for streamlined and automated training

**Reputation / proof points**
* Coverage in US, EU, JP, AU
* Supports multiple languages including English, German, French, Spanish, Japanese, and Chinese.

Additional information

Veeva Systems offers solutions aimed at achieving and maintaining TMF (Trial Master File) inspection readiness. Their platform is designed to streamline clinical research processes, from site activation and payments to data management and training. By centralizing information and automating workflows, Veeva aims to provide a constant state of readiness for regulatory inspections. Key functionalities include faster site payments, efficient trial management, and improved investigator data management. Their approach focuses on modernizing eTMF systems to ensure continuous compliance and operational efficiency.

Key Highlights

  • Offers Veeva eTMF to help maintain a constant state of TMF inspection readiness. Source
    “Veeva eTMFStay inspection ready”
  • Provides Veeva Payments to pay clinical research sites faster. Source
    “Veeva PaymentsPay clinical research sites faster”
  • Streamlines and automates training with Veeva Study Training. Source
    “Veeva Study TrainingStreamline and automate training”
  • Automates information sharing with Veeva Site Connect. Source
    “Veeva Site ConnectAutomate information sharing”

Certifications & Trust Signals

  • Veeva Systems provides the industry cloud for life sciences. Source
    “Veeva Systems provides the industry cloud for life sciences”

Buyer Snapshot

Best for
  • Life sciences organizations seeking to improve clinical operations efficiency
  • Companies preparing for regulatory inspections
  • Organizations needing to modernize their TMF and eTMF systems
How engagement typically works
  • Software-as-a-Service (SaaS) platform
  • Focus on end-to-end trial management solutions
Typical deliverables
  • Veeva eTMF platform
  • Veeva CTMS
  • Veeva Payments
  • Veeva Study Startup
  • Veeva RTSM
  • Veeva Site Connect
Good to know
  • Best when integrated within the Veeva ecosystem for maximum benefit.
HQ: Pleasanton, US
Languages: English, German, French, Spanish, Japanese, Chinese
Timezones: PST, EST, GMT, CET, JST
Status: listed

Services & Capabilities

FDA QMSR Transition & Inspection Readiness (ISO 13485 Alignment)

Jurisdictions: US, EU, JP, AU
Countries: US, UK, Germany, France, Japan, China
Industries: Medical Devices, IVD, Pharmaceuticals, Biotech
Onboarding time: 14–28 days
Pricing model: Custom pricing
Service Types: Mock FDA Inspection

Additional fda_qmsr_transition_inspection_readiness Details

Service Types
Mock FDA Inspection, Training & Competency Programs
Earliest Start
flexible
Delivery Mode
Hybrid
Inspection Experience
Supports mock inspections regularly
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