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.
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...
We acknowledge the inherent diversity in workflows, processes, and reporting prerequisites across life sciences businesses. Hence, we present our impeccable customization...
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...
In the heavily regulated life sciences industry, compliance is essential. ProPharma comprehends the intricate web of regulatory requirements that envelop the...
Technology and processes are constantly evolving. Our dedicated team delivers regular system maintenance, expert troubleshooting, and responsive Vault business...
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.
September 4, 2025
Discover strategies to enhance efficiency and quality in high-volume medical information contact centers, reducing call strain while improving customer satisfaction and agent performance.
September 3, 2025
Discover how our MAH expertise in Eastern Europe ensures seamless regulatory compliance, lifecycle management, and strategic market entry.
September 2, 2025
Reduce delays & risks: streamline your MLR submissions with ProPharma’s expert checklist. Prepare materials that minimize delays, reduce risks, and accelerate approvals.
July 8, 2025
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 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 CFO to drive financial strategy and accelerate global growth, leveraging his 20 years of life sciences industry experience.
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