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Boehringer Ingelheim Partners with Veeva to Advance its Clinical and Regulatory Operations in Animal Health

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Boehringer Ingelheim adopts Veeva Vault Clinical and Veeva Vault RIM for streamlined clinical and regulatory management in its animal health business unit, aiming to accelerate the development of new medicines for animals and improve operational efficiency.
Positive
  • Boehringer Ingelheim selects Veeva Vault Clinical and Veeva Vault RIM for clinical and regulatory management.
  • Unified applications on a single platform to streamline clinical execution for faster development of new medicines.
  • Veeva solutions aim to drive higher operational efficiency and data-driven decision making.
  • Boehringer Ingelheim to use Veeva Vault CTMS and eTMF for trial management and inspection readiness.
  • Vault RIM applications for advanced regulatory processes and seamless information exchange.
  • Establishing a centralized digital foundation with Veeva for better user experience and lean processes.
  • Partnership with Veeva to increase data integrity and adaptability to changing business requirements.
Negative
  • None.

Global animal health leader adopts Veeva Vault Clinical and Veeva Vault RIM for greater efficiency, visibility, and speed

PLEASANTON, Calif., Feb. 14, 2024 /PRNewswire/ -- Veeva Systems (NYSE: VEEV) today announced that Boehringer Ingelheim has selected Veeva Vault Clinical and Veeva Vault RIM applications as its technology foundation for clinical and regulatory management in its animal health business unit. By adopting unified applications on a single platform, Boehringer Ingelheim can streamline clinical execution to speed development of new medicines that help animals live healthier and happier lives.

"Veeva Vault Clinical and Veeva Vault RIM will help us drive higher operational efficiency across functions while providing the insights for data-driven decision making," said Marcus Gravendyck, head of global regulatory affairs and pharmacovigilance, Animal Health at Boehringer Ingelheim. "This will allow us to execute and innovate faster to improve the lives of animals."

Boehringer Ingelheim will use Veeva Vault CTMS in its animal health business unit to manage and monitor trials and Veeva Vault eTMF for real-time inspection readiness, visibility, and control. The company will also use Vault RIM applications, including Veeva Vault Registrations, Veeva Vault Submissions, and Veeva Vault Submissions Archive for advanced regulatory processes. Connecting these applications on a single cloud platform will enable real-time access to data and seamless information exchange.

"Boehringer Ingelheim is driving innovation to accelerate the development of new treatments for animals," said Thomas Reith, corporate vice president, IT research, development, and medicine at Boehringer Ingelheim. "By establishing a centralized and digital foundation with Veeva, we can deliver a better user experience for our teams, and offer lean, end-to-end processes for speed and agility."

"We're proud to partner with Boehringer Ingelheim in animal health to simplify their clinical development and regulatory processes," said Stefan Jahnecke, vice president of animal health strategy at Veeva. "Veeva Vault Clinical and Veeva Vault RIM will help Boehringer Ingelheim increase data integrity and provide the visibility to quickly adapt to changing business requirements."

Vault Clinical and Vault RIM are part of Veeva Development Cloud, the technology foundation for product development across clinical, regulatory, quality, and safety. To learn more, visit veeva.com/DevelopmentCloud.

About Veeva Systems
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world's largest biopharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. For more information, visit veeva.com.

Veeva Forward-looking Statements
This release contains forward-looking statements regarding Veeva's products and services and the expected results or benefits from use of our products and services. These statements are based on our current expectations. Actual results could differ materially from those provided in this release and we have no obligation to update such statements. There are numerous risks that have the potential to negatively impact our results, including the risks and uncertainties disclosed in our filing on Form 10-Q for the period ended October 31, 2023, which you can find here (a summary of risks which may impact our business can be found on pages 38 and 39), and in our subsequent SEC filings, which you can access at sec.gov.

Contact:


Deivis Mercado
Veeva Systems
925-226-8821
deivis.mercado@veeva.com

Jeremy Whittaker
Veeva Systems
+49-695-095-5486
jeremy.whittaker@veeva.com

 

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SOURCE Veeva Systems

FAQ

What technology foundation has Boehringer Ingelheim adopted for clinical and regulatory management in its animal health business unit?

Boehringer Ingelheim has selected Veeva Vault Clinical and Veeva Vault RIM applications as its technology foundation.

What are the benefits of adopting unified applications on a single platform for Boehringer Ingelheim?

Unified applications on a single platform help streamline clinical execution for faster development of new medicines and drive higher operational efficiency.

Which Veeva solutions will Boehringer Ingelheim use in its animal health business unit for trial management and inspection readiness?

Boehringer Ingelheim will use Veeva Vault CTMS for trial management and Veeva Vault eTMF for real-time inspection readiness.

What applications will Boehringer Ingelheim use for advanced regulatory processes?

Boehringer Ingelheim will use Vault RIM applications, including Veeva Vault Registrations, Veeva Vault Submissions, and Veeva Vault Submissions Archive, for advanced regulatory processes.

Who is the head of global regulatory affairs and pharmacovigilance, Animal Health at Boehringer Ingelheim?

Marcus Gravendyck is the head of global regulatory affairs and pharmacovigilance, Animal Health at Boehringer Ingelheim.

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