VVodori provides cloud-based software for life sciences to manage the review and distribution of promotional materials. Its Pepper Flow speeds and standardizes review workflows, while Pepper Flow Digital Review replaces PDF reviews with interactive web-based page reviews. Accessed via subscription, the platform supports remote teams and helps pharmaceutical, biotechnology, and medical device companies stay compliant and keep sales teams up to date. The goal is to accelerate compliant marketing processes by centralizing review and distribution of approved assets.
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Company Size
51-200
Company Stage
Series A
Total Funding
$10.8M
Headquarters
Chicago, Illinois
Founded
2005
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Vodori launches Salesforce Agentforce Life Sciences app to connect approved content with customer engagement. App automatically synchronizes approved content from Vodori into Salesforce, accelerating activation, reducing manual administration, and preserving governance CHICAGO, IL, UNITED STATES, September 29, 2026 / EINPresswire.com / - Vodori, a provider in cloud-based software for compliant content review and approval in the life sciences industry, today announced the launch of its newest application for Salesforce Agentforce Life Sciences on AgentExchange. The application creates a governed path from content approval to customer engagement by automatically synchronizing approved content and associated metadata from Vodori into Salesforce Agentforce Life Sciences. Commercial and medical teams can access current materials directly in Salesforce, reducing manual uploads, administrative effort, and versioning risk. Consistent with Vodori's core platform and other Salesforce connectors, the Agentforce Life Sciences app ships pre-validated by Vodori, providing robust GxP software quality assurance to this critical data process. The launch builds on Vodori's strategy emphasizing customer choice around the commercial tech stack, connecting approved content to leading sales enablement and CRM platforms. "We believe life sciences organizations should be able to assemble a digital ecosystem from the platforms that best meet their needs without taking on the burden of connecting and maintaining those systems themselves," said Scott Rovegno, CEO of Vodori. "Vodori created a productized, vendor-supported connection between regulated content and customer engagement. Customers gain the flexibility of an open ecosystem with the reliability, accountability, and long-term support they expect from an enterprise platform." Vodori and Salesforce address different, but closely connected, parts of the content lifecycle. Vodori helps organizations review, approve, govern, and manage regulated content. Salesforce gives commercial and medical teams a platform for collaborating, engaging healthcare professionals, and managing customer relationships. The new application connects those environments by making approved content and its associated metadata available directly within Salesforce Agentforce Life Sciences. This gives life sciences organizations a practical path to modernizing content operations without giving up compliance controls. FROM APPROVAL TO ACTIVATION For many life science organizations, the process for bringing content to market breaks down after content approval. Marketing teams may review and approve content in one system, while commercial and medical teams retrieve it from another. Content is uploaded manually, versions become difficult to track, and approved materials take longer than they should to reach the people who need them. Vodori connects those two parts of the process. Key capabilities include: - Automatically syncing approved content and related metadata into Salesforce Agentforce Life Sciences - Giving commercial and medical teams access to current, approved materials - Removing expired or withdrawn content automatically - Using existing Salesforce permissions to control access - Reducing manual administration while preserving governance throughout the content lifecycle The Vodori Agentforce Life Sciences application is available through Salesforce AgentExchange. About Vodori Vodori helps life sciences organizations create, review, approve, and activate compliant content through an AI-powered platform purpose-built for life science teams. Building on more than 20 years of MLR expertise, Vodori is evolving that foundation through the creation of the Regulated Content Intelligence Platform(TM)(RCIP), the first enterprise software category purpose-built to operationalize governed knowledge across the regulated content lifecycle. Annalise Ludtke Vodori +1 269-808-0012 email Healthcare Industry Today here Legal Disclaimer: EIN Presswire provides this news content "as is" without warranty of any kind. Healthcare Industry Today do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.
Vodori, creator of the Regulated Content Intelligence Platform, has appointed Becki Morison to its board of directors. Morison, CEO of Essential Pharma, joined the board in August 2026. Morison brings over 25 years of international pharmaceutical leadership experience, spanning commercial strategy, organisational transformation, medical affairs, and pricing. Based in London, she will support Vodori's expansion across Europe, working with Ross Grey, the company's VP and GM for EMEA. Vodori provides an AI-powered platform helping life sciences organisations create, review, approve, and activate compliant content. The company has built upon more than 20 years of MLR expertise to develop its platform for regulated content lifecycle management.
Vodori has launched what it calls the Regulated Content Intelligence Platform (RCIP), describing it as a new enterprise software category for life sciences. The platform combines a system of record for governed knowledge with AI-powered assistance for authoring, reviewing, approving, and distributing regulated content. RCIP embeds AI within the regulated content lifecycle, applying approved claims, scientific evidence, references, and compliance policies throughout the process. The first capability, Content Preflight, identifies spelling, grammar, formatting, and branding issues before formal Medical, Legal, and Regulatory review begins. According to Vodori's 2025 benchmarks report, nearly half of promotional content recirculation stems from preventable issues. The platform aims to reduce unnecessary review cycles whilst allowing reviewers to focus on scientific accuracy and regulatory decisions. Vodori plans to roll out additional capabilities through 2027, including Claims Intelligence in October and Regulatory Intelligence in early 2027. The company launched an Innovation Partner Programme in Q2 to help validate the platform architecture.
Vodori and BridgeView announce strategic partnership to transform content review across the life science industry. Turnkey MLR solution enables 30-60% faster review cycles with compliance and scalability built in CHICAGO, IL, UNITED STATES, January 8, 2026 /EINPresswire.com/ - Vodori, the leading provider of cloud-based compliant content management solutions for life sciences, and Bridgeview, a full-service consulting partner and a Zensar company, today announced a new partnership focused on helping life sciences companies modernize and streamline their promotional and medical content review process. The partnership combines Vodori's proven Medical-Legal-Regulatory Content Review (MLR) technology with BridgeView's regulatory expertise and implementation support to offer complete, compliant, and scalable solutions for teams across pharma, biotech, and medtech. Whether preparing for launch, expanding into new markets, or replacing legacy systems, life sciences companies can now simplify their MLR operations and accelerate time-to-approval. Together, Vodori and Bridgeview deliver a solution that includes: - A validated, compliance-ready MLR platform: Vodori's platform provides 21 CFR Part 11 and EU Annex 11 compliance, audit-ready workflows, real-time cross-functional collaboration, and modern digital content review. Customers reduce review cycles by 30 - 60%, enabling faster market execution. - Expert-led implementation, SOP guidance, and change management: Bridgeview complements the technology with hands-on configuration and implementation services, SOP development, training, content migration, and change management support tailored to the unique needs of life science teams. "Life sciences companies of all sizes deserve the same level of compliance confidence and delivery speed," said Scott Rovegno, Founder and CEO at Vodori. "Our partnership with BrideView brings together scalable technology and deep domain expertise to help customers modernize how they manage content and do it without complexity or delays." Mihales Karasavas, CCO, BridgeView Life Sciences, added, "Every day counts toward a patient receiving a life-changing therapy and BridgeView is dedicated to bringing world-class digital transformation to the life sciences sector. By pairing Vodori's MLR technology with our deep operational expertise, we are giving our clients a scalable, end-to-end framework to launch faster while ensuring compliance foundational to their success." Both Vodori and BridgeView have been recognized by Salesforce as Life Science Cloud partners, reinforcing their leadership in delivering modern, integrated solutions across the ecosystem. Life sciences organizations interested in accelerating compliant content review and simplifying MLR operations can learn more at vodori.com. About Vodori Vodori delivers cloud-based software that helps life sciences companies bring compliant content to market faster. We help commercial, clinical, regulatory, and quality functions streamline the review, approval, and distribution of promotional, scientific, and medical content. Vodori supports emerging, SMB, and enterprise customers across the globe and is Salesforce's exclusive MLR partner for Life Sciences Cloud. Follow Vodori via: Vodori Blog: https://www.vodori.com/blog LinkedIn: https://www.linkedin.com/company/vodori Website: www.vodori.com About Zensar At Zensar, we are 'experience-led everything.' We conceptualize, design, engineer, market, and manage digital solutions and experiences for 145+ leading enterprises. Using our 3Es of experience, engineering, and engagement, we harness the power of technology, creativity, and insight to deliver impact. Part of the $4.8 billion RPG Group, we are headquartered in Pune, India. Our 10,000+ employees work across 30+ locations worldwide, including Milpitas, Seattle, Princeton, Zurich, Cape Town, London, Singapore, and Mexico City. Follow Zensar via: Zensar Blog: http://www.zensar.com/blogs Twitter: https://twitter.com/Zensar LinkedIn: https://www.linkedin.com/company/zensar-technologies Facebook: https://www.facebook.com/ZensarTech/ Website: www.zensar.com Annalise Ludtke Vodori +1 269-808-0012 [email protected] EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above. Information contained on this page is provided by an independent third-party content provider. XPRMedia and this Site make no warranties or representations in connection therewith. If you are affiliated with this page and would like it removed please contact [email protected]
Tact.ai, a Sunnyvale, Calif.-based provider of customer engagement software to life science organizations, added $33 million in a new round of funding from dRx Capital, M12, Salesforce Ventures, Eli Lilly & Co. and McKesson Ventures.
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Industries
Company Size
51-200
Company Stage
Series A
Total Funding
$10.8M
Headquarters
Chicago, Illinois
Founded
2005
Find jobs on Simplify and start your career today