Veeva Vault Support Services

Unlock the Full Potential of Veeva's Vault Platform with ProPharma's Comprehensive Services

Veeva Services Partner Certified Commercial Cloud Badge 2024

Maximize the power of Veeva's platform for your life sciences business with the unparalleled support and expertise of ProPharma. As a distinguished certified Veeva services partner, we offer an array of services meticulously crafted to optimize your Veeva Vault applications and ensure alignment with your organization's processes.

Veeva Vault Support Expertise

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Unmatched Veeva Consulting Expertise

Our experienced team of Veeva consultants and experts possess an extensive track record of working seamlessly with the platform. Rely on our profound knowledge to...

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Unmatched Veeva Consulting Expertise

Our experienced team of Veeva consultants and experts possess an extensive track record of working seamlessly with the platform. Rely on our profound knowledge to comprehend the platform's multifaceted capabilities, craft new workflows, and optimize the system to precisely align with your distinct business requirements.

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Tailored Customization

We acknowledge the inherent diversity in workflows, processes, and reporting prerequisites across life sciences businesses. Hence, we present our impeccable customization...

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Tailored Customization

We acknowledge the inherent diversity in workflows, processes, and reporting prerequisites across life sciences businesses. Hence, we present our impeccable customization services to assist you in tailoring the Veeva platform to optimally suit your unique needs. Our adept professionals can engineer custom workflows, seamlessly integrate the platform with other systems, and construct tailor-made reports, ensuring that Veeva Vault harmonizes with your business ecosystem and processes.

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Empowering Veeva Training Programs

To get the most out of Veeva, your employees need to be fully equipped to use it effectively. That's why we provide Veeva training services to help your team become...

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Empowering Veeva Training Programs

To get the most out of Veeva, your employees need to be fully equipped to use it effectively. That's why we provide Veeva training services to help your team become Veeva experts. We offer on-site, virtual, and customized training programs that can be tailored to your specific needs. With our Veeva training program, you can ensure that your team is using Veeva to its fullest potential.

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Adhering to Regulatory Compliance

In the heavily regulated life sciences industry, compliance is essential. ProPharma comprehends the intricate web of regulatory requirements that envelop the...

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Adhering to Regulatory Compliance

In the heavily regulated life sciences industry, compliance is essential. ProPharma comprehends the intricate web of regulatory requirements that envelop the industry, and we are here to help you navigate the complex landscape. Our compliance expertise empowers you to confidently ensure that your Veeva platform meets all necessary regulatory standards, fostering peace of mind and promoting a secure and compliant environment.

Our experts can take the lead on system validation, development of SOPs, Work Instruction, and Job Aids, and lead ongoing change control, giving your organization the peace of mind of knowing that the system is maintained in a validated state.

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Managed Veeva Services and Support

Technology and processes are constantly evolving. Our dedicated team delivers regular system maintenance, expert troubleshooting, and responsive Vault business...

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Managed Veeva Services and Support

Technology and processes are constantly evolving. Our dedicated team delivers regular system maintenance, expert troubleshooting, and responsive Vault business administration services, ensuring that your Veeva platform consistently performs at peak efficiency. From User Access Management to performing Upgrade Impact Assessments and new feature enablement, our experts ensure that your organization gets the most out of your Veeva Vault applications.

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Veeva Vault Product Support

ProPharma implements and supports a wide range of Veeva products. Below are examples of how we support Sponsors on a select few Veeva applications.

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Veeva EDC

Veeva EDC

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Veeva CTMS

Veeva CTMS

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Veeva QMS

Veeva QMS

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Veeva eTMF

Veeva eTMF

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Veeva RIM

Veeva RIM

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Veeva CDMS

Veeva CDMS

Veeva Vault EDC

ProPharma offers comprehensive, end-to-end support for Veeva Vault EDC, focusing on optimizing electronic data capture in clinical trials. Our clinical programmers expertly develop study specifications, build intuitive user interfaces, and implement effective edit checks to ensure data quality. We ensure efficient implementation and configuration by developing global study libraries that streamline data collection processes, enhance accuracy, and ensure compliance. Through system and study-level validation, ongoing maintenance, and tailored training, we help clients fully harness Vault EDC’s capabilities, ultimately improving trial efficiency and accelerating study timelines while adhering to regulatory requirements.

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Veeva Vault CTMS

ProPharma offers specialized services for Veeva Vault CTMS, helping life sciences organizations streamline clinical trial management. By configuring and integrating Vault CTMS, ProPharma ensures efficient planning, tracking, and reporting across trial operations. Our support includes system validation, system integration, study startup, and workflow customization, enabling clients to manage trial data more effectively while maintaining compliance with global regulatory requirements. With our expertise, clients can improve trial visibility, coordination, and overall performance, driving faster and more informed decision-making throughout the clinical study lifecycle.

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Veeva Vault QMS

ProPharma delivers expert services for Veeva Vault QualityDocs and QMS, focusing on optimizing quality management processes for life sciences organizations. By tailoring and integrating Vault QMS, ProPharma helps clients manage quality events, deviations, audits, and CAPAs more efficiently while ensuring compliance with industry standards. Our team provides comprehensive support, including SOP development, system validation, workflow customization, and training, to enhance the functionality and effectiveness of quality management systems. With our expertise, clients can maintain a higher standard of quality control and streamline their operations across the product lifecycle.

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Veeva Vault eTMF

ProPharma offers tailored support for Veeva Vault eTMF, helping life sciences organizations streamline their trial master file processes. Our team ensures efficient implementation and configuration of Vault eTMF, allowing clients to maintain real-time inspection readiness and improve collaboration across teams. Through system validation, ongoing maintenance, and customized training, we enable companies to optimize their document management, ensuring compliance with regulatory standards. ProPharma’s expertise ensures that clinical trial documentation is well-organized, accessible, and aligned with best practices for trial oversight and governance.

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Veeva Vault RIM

ProPharma supports Veeva Vault RIM by delivering tailored solutions that enhance regulatory information management and compliance. Leveraging our extensive experience with Veeva Vault platform and our regulatory expertise, we help organizations integrate and optimize Vault RIM to manage submission processes, regulatory records, and product registrations efficiently. ProPharma's experts ensure your systems are configured to meet global regulatory requirements, providing end-to-end support that includes data migration, system validation, archiving, and training. This enables clients to streamline operations, improve visibility, and accelerate time to market for their products.

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Veeva Vault CDMS

ProPharma provides comprehensive support for Veeva Vault CDMS, helping life sciences companies optimize their clinical data management processes. Our team specializes in the configuration and implementation of Vault CDMS, streamlining data workflows for greater efficiency and accuracy in clinical trials. We offer services that include system validation, data migration, training, and ongoing support to ensure smooth operations and regulatory compliance. With our expertise, clients can leverage Vault CDMS to improve data quality, accelerate trial timelines, and enhance overall clinical data management.

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Partner with ProPharma for Veeva Services Excellence

With ProPharma as your trusted Veeva services partner, embark on a journey of successful implementation, streamlined operations, and complete alignment with your business imperatives. Contact us today to discover more about our exceptional offerings or engage in a conversation with one of our esteemed experts. Experience the ProPharma advantage and unlock the true potential of Veeva for your life sciences enterprise.

News & Insights

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WHO Issues Guidance on Antibiotic Pollution Control

WHO issues guidance to control antibiotic pollution from manufacturing, addressing environmental and global health impacts of antimicrobial resistance.

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Nonclinical Drug Development: FDA Recommendations for Confirming an Ames Positive Finding

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ProPharma Appoints Brian Tuttle as Chief Financial Officer

October 21, 2024

ProPharma Appoints Brian Tuttle as Chief Financial Officer

ProPharma appoints Brian Tuttle as CFO to drive financial strategy and accelerate global growth, leveraging his 20 years of life sciences industry experience.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Names Dawn Sherman Chief Executive Officer

September 30, 2024

ProPharma Names Dawn Sherman Chief Executive Officer

Dawn Sherman rejoins ProPharma as CEO, bringing nearly 30 years of industry experience to lead the regulatory, clinical, and compliance services provider.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

ProPharma Receives 2024 CRO Leadership Award

June 13, 2024

ProPharma Receives 2024 CRO Leadership Award

ProPharma wins 2024 CRO Leadership Award for exceeding expectations in key categories, solidifying its position as a top global research consulting organization in the life sciences industry.

Infographic The Cost of Poor Project Management - ProPharma

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The Cost of Poor Project Management

Project Management isn’t for the faint of heart. There is a shockingly high rate of project failure… but on the other hand, great project management can be a key differentiator that leads a company...

Infographic Successfully Passing MHRA Inspections for Overseas Manufacturing Sites - ProPharma

August 31, 2022

Successfully Passing MHRA Inspections for Overseas Manufacturing Sites

ProPharma offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. ProPharma’s Compliance and Quality team completed the first on-site...

Infographic Navigating the Generic Drug Application and Approval Process - ProPharma

October 4, 2021

Navigating the Generic Drug Application and Approval Process

Navigating the generic drug application and approval process can be challenging. From pre-filing through post-approval, find out exactly what needs to be done for your Abbreviated New Drug...

News & Insights

ProPharma Appoints Brian Tuttle as Chief Financial Officer

October 21, 2024

ProPharma Appoints Brian Tuttle as Chief Financial Officer

ProPharma appoints Brian Tuttle as CFO to drive financial strategy and accelerate global growth, leveraging his 20 years of life sciences industry experience.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Names Dawn Sherman Chief Executive Officer

September 30, 2024

ProPharma Names Dawn Sherman Chief Executive Officer

Dawn Sherman rejoins ProPharma as CEO, bringing nearly 30 years of industry experience to lead the regulatory, clinical, and compliance services provider.

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ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

ProPharma Receives 2024 CRO Leadership Award

June 13, 2024

ProPharma Receives 2024 CRO Leadership Award

ProPharma wins 2024 CRO Leadership Award for exceeding expectations in key categories, solidifying its position as a top global research consulting organization in the life sciences industry.

Previous Award Arrow Next Award Arrow
WHO Issues Guidance on Antibiotic Pollution Control

December 19, 2024

WHO Issues Guidance on Antibiotic Pollution Control

WHO issues guidance to control antibiotic pollution from manufacturing, addressing environmental and global health impacts of antimicrobial resistance.

Nonclinical Drug Development: FDA Recommendations for Confirming an Ames Positive Finding

December 18, 2024

Nonclinical Drug Development: FDA Recommendations for Confirming an Ames Positive Finding

Explore FDA's recommendations on follow-up testing for Ames-positive drugs to support first-in-human clinical trials. Learn how to navigate FDA regulations and ensuring successful product development.

Navigating Market Access & Reimbursement Strategy for Medical Devices in Europe

December 17, 2024

Navigating Market Access & Reimbursement Strategy for Medical Devices in Europe

Explore the importance of market access and reimbursement strategies for medical devices and in vitro diagnostics (IVDs) in Europe. Learn how early planning and the new European HTAR can enhance the...

Previous Post Arrow Next Post Arrow
Infographic The Cost of Poor Project Management - ProPharma

June 10, 2022

The Cost of Poor Project Management

Project Management isn’t for the faint of heart. There is a shockingly high rate of project failure… but on the other hand, great project management can be a key differentiator that leads a company...

Infographic Successfully Passing MHRA Inspections for Overseas Manufacturing Sites - ProPharma

August 31, 2022

Successfully Passing MHRA Inspections for Overseas Manufacturing Sites

ProPharma offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. ProPharma’s Compliance and Quality team completed the first on-site...

Infographic Navigating the Generic Drug Application and Approval Process - ProPharma

October 4, 2021

Navigating the Generic Drug Application and Approval Process

Navigating the generic drug application and approval process can be challenging. From pre-filing through post-approval, find out exactly what needs to be done for your Abbreviated New Drug...

Previous Resource Arrow Next Resource Arrow