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
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...
Tailored Customization
We acknowledge the inherent diversity in workflows, processes, and reporting prerequisites across life sciences businesses. Hence, we present our impeccable customization...
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...
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...
Managed Veeva Services and Support
Technology and processes are constantly evolving. Our dedicated team delivers regular system maintenance, expert troubleshooting, and responsive Vault business...
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.
News & Insights
July 25, 2025
Understanding the Roles of LPPV, QPPV, and the PSMF in Pharmacovigilance: A Guid...
Learn about the crucial roles of QPPV, LPPV, and PSMF in ensuring effective pharmacovigilance and regulatory compliance for Marketing Authorization Holders (MAHs).
July 24, 2025
FDA Publishes over 200 Complete Response Letters (CRLs)
FDA's new transparency with over 200 CRLs empowers sponsors to navigate regulatory challenges more effectively, accelerating drug approvals and enhancing patient access to treatments.
July 24, 2025
Navigating EMA and Global Regulations for Medical Information Services
ProPharma guides clients through global medical information regulatory landscapes, ensuring compliance and excellence across markets with tailored solutions, AI integration, and continuous training.
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News & Insights
July 8, 2025
ProPharma Appoints Marshall Florence, Former FDA Labeling Expert, as Vice Presid...
ProPharma appoints former FDA labeling expert as VP, Labeling & Strategy, enhancing strategic labeling, promotional review, and regulatory consulting expertise to accelerate drug development and...
January 31, 2025
ProPharma Recognized for AI Excellence at ECCCSA
ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.
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.
