Veeva Vault RIM
Veeva Systems Inc
Veeva Systems Inc. offers expert training and certification for life sciences professionals, empowering teams to become Veeva experts and optimize platform use for enhanced productivity and compliance.
Veeva Systems Inc. provides comprehensive training and certification programs designed to equip life sciences professionals with the knowledge and skills to maximize the potential of Veeva solutions. Their offerings focus on improving productivity, ensuring compliance, and driving success within the dynamic life sciences industry. Courses are structured to impart in-depth knowledge and practical skills, enabling individuals and teams to become proficient in Veeva platforms, thereby elevating career prospects and organizational performance. The company's services extend to streamlining clinical operations, including the management of clinical trials, site activation, and training processes. Veeva's solutions aim to centralize data, automate workflows, and enhance reporting and analysis, supporting end-to-end clinical trial management and ensuring inspection readiness. They are trusted by the industry to deliver solutions that support long-term success and operational efficiency.
About
**Who they are**
Veeva Vault RIM is a provider of expert training and certification for life sciences professionals, focused on optimizing platform use for enhanced productivity and compliance. They empower teams to become Veeva experts.
**Expertise & scope**
* Streamline and automate training
* Centralize clinical trial disclosures
* Provide investigator and site data
* Pay clinical research sites faster
* Randomization and supply management
* Accelerate site activation
* Automate information sharing
* Manage trials end-to-end
* Stay inspection ready
**Reputation / proof points**
* Trusted by the Industry Since 2007
Veeva Vault RIM is a provider of expert training and certification for life sciences professionals, focused on optimizing platform use for enhanced productivity and compliance. They empower teams to become Veeva experts.
**Expertise & scope**
* Streamline and automate training
* Centralize clinical trial disclosures
* Provide investigator and site data
* Pay clinical research sites faster
* Randomization and supply management
* Accelerate site activation
* Automate information sharing
* Manage trials end-to-end
* Stay inspection ready
**Reputation / proof points**
* Trusted by the Industry Since 2007
Additional information
Veeva Services focuses on empowering life sciences professionals through expert training and certification. Their offerings are designed to enhance platform utilization, leading to improved productivity and adherence to compliance standards. Key areas of focus include streamlining training processes, centralizing clinical trial disclosures, and providing essential investigator and site data. They also offer solutions for faster clinical research site payments, randomization and supply management, and accelerating site activation. Their platform supports end-to-end trial management and helps teams stay inspection-ready.
Key Highlights
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Trusted by the Industry Since 2007
Source
“Trusted by the Industry Since 2007”
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Streamline and automate training
Source
“Streamline and automate training”
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Centralize clinical trial disclosures
Source
“Centralize clinical trial disclosures”
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Provide investigator and site data
Source
“Provide investigator and site data”
Certifications & Trust Signals
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Trusted by the Industry Since 2007
Source
“Trusted by the Industry Since 2007”
Buyer Snapshot
Best for
- Life sciences professionals seeking platform expertise
- Organizations aiming to optimize clinical trial processes
How engagement typically works
- Training and certification programs
- Platform optimization services
Typical deliverables
- Streamlined training workflows
- Centralized disclosure management
- Improved site data management
- Faster site payments
- Enhanced trial management
Good to know
- Best when focused on leveraging Veeva platform capabilities
HQ:
Radnor, US
Languages:
English
Timezones:
America/New_York
Status:
listed
Services & Capabilities
Best EUDAMED Registration| Compare & Get Quotes
Jurisdictions:
EU
Countries:
DE, AT, BE, IT, IE, NL, ES
Industries:
Medical devices, IVD, SaMD, Manufacturing
Portfolio:
100+
Onboarding time:
2–14 days
Pricing model:
Usage-based
Starting from:
USD 1,500
Included services:
Actor/SRN registration support, UDI/Device module readiness, Data preparation & validation, Training enablement
Supports Training Enablement:
Yes
Modules Supported:
Clinical investigations
Additional eudamed_reg_support Details
Included Services Detailed
Actor/SRN registration readiness review and submission support (seed scope), UDI/Device data preparation, validation, and upload workflow support (seed scope), Internal data governance mapping (roles, owners, approvals) (seed scope), Training enablement for EUDAMED operational tasks (seed scope)
Excluded Services
Notified Body services or conformity assessment decision-making, Legal representation with Competent Authorities, Clinical evaluation or performance evaluation writing (unless separately scoped)
Onboarding Steps
The provided website content does not detail specific onboarding steps for EUDAMED registration support.
Data Load Notes
Data load support level indicates whether uploads are done-for-you, guided, or training-only (seed summary).
Supports Actor Registration
false
Supports UDI
false
Supports Vigilance
false
Supports Clinical Investigations
false
Modules Supported
UDI/Devices, Vigilance, Clinical Investigations, Certificates & Notifications
