Leading Companies Transform Regulatory Processes with Veeva
Accelerating Market Entry through Veeva RIM
As the landscape of life sciences continues to evolve, more than 450 companies are embracing innovative solutions to enhance their regulatory processes. Veeva Systems (NYSE: VEEV) has emerged as a vital player, offering advanced regulatory capabilities that foster collaboration with global health authorities.
Innovative Partnerships Fueling Transformation
The need for speed and efficiency in regulatory information management (RIM) has never been more pressing. Companies now recognize that adopting technologies like Veeva RIM facilitates a unified platform for managing their regulatory lifecycle. This platform is already in use by 19 of the top 20 biopharmaceutical companies, showcasing its pivotal role in the industry.
Enhancing Connectivity and Compliance
Veeva's drive for innovation has led to strategic partnerships with key organizations such as Accumulus Technologies and DNAnexus. These collaborations are designed to interlink with multiple health authority platforms, enhancing operational efficiency and regulatory compliance across diverse markets.
According to Marc Gabriel, vice president of regulatory at Veeva, the integration of these products allows for significant improvements in efficiency, cutting down on crucial cycle times. Veeva RIM provides an invaluable end-to-end solution that not only accelerates market entry but also enhances collaboration among global stakeholders.
Streamlined Processes for Effective Submissions
One of the core strengths of Veeva RIM is its ability to refine processes throughout the regulatory lifecycle. This is evident with the implementation of Veeva Submissions Publishing, where over 85 organizations leverage continuous publishing to minimize rework and eliminate bottlenecks, which in turn speeds up submission timelines.
Empowering Regulatory Submissions
The partnership with Accumulus aims to modernize regulatory information sharing by connecting its platform with Veeva RIM. This interchange ensures that information is readily accessible and shareable among a network of over 70 regulatory agencies globally, expediting the process of getting treatments to patients.
DNAnexus also enhances Veeva RIM with its Trusted Regulatory Spaces (TRS) feature, which is focused on best-in-class data sharing capabilities. This integration is expected to streamline collaboration between different agencies and promote quicker approvals for regulated products.
Veeva Development Cloud: A Comprehensive Solution
At the core of these advancements is the Veeva Development Cloud, which provides a comprehensive technology framework for product development. This cloud-based platform consolidates clinical, quality, regulatory, and safety management into a single solution, promoting operational fluidity and ensuring that companies can meet the stringent demands of the regulatory environment.
About Veeva Systems
Veeva Systems is dedicated to offering industry-specific cloud services tailored for life sciences. The company supports over 1,500 clients ranging from leading biopharmaceutical giants to emerging biotechs. By focusing on innovation and excellence in service, Veeva maintains a strong commitment to the success of its customers.
As a Public Benefit Corporation, Veeva prioritizes balancing stakeholder interests, thus creating value not only for its clients but also for employees and shareholders. To learn more about their offerings, visit the Veeva website.
Frequently Asked Questions
What is Veeva RIM?
Veeva RIM is a regulatory information management platform that helps life sciences companies streamline and manage their regulatory processes effectively.
How many companies are using Veeva RIM?
Over 450 companies, including 19 of the top 20 biopharmaceutical firms, have adopted Veeva RIM for their regulatory information management needs.
What benefits do partnerships with Accumulus and DNAnexus provide?
The partnerships enhance interoperability, allowing for more efficient data sharing and collaboration among regulatory agencies, ultimately accelerating product approvals.
How does Veeva Submissions Publishing improve regulatory processes?
By implementing continuous publishing, Veeva Submissions Publishing reduces rework and bottlenecks, leading to faster submission timelines for companies.
What is the Veeva Development Cloud?
Veeva Development Cloud is a comprehensive technology foundation that integrates clinical, regulatory, quality, and safety management into a unified platform for product development.
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