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Company description
Nextrove is a life sciences professional services and solutions firm focused exclusively on Pharmaceutical, Biotech, and Contract Research Organizations. Headquartered in Princeton, New Jersey, with offices in the UK (Leicester), Italy (Milan), Japan (Tokyo), China (Shanghai), South Korea (Seoul), and India (Noida, Bengaluru, and Mysuru), the company draws on over 20 years of experience to help clients meet global digitalization strategies, maintain regulatory compliance, and reduce total cost of ownership. Its stated mission is to improve patient safety through consulting, technology implementation, and managed services across pharmacovigilance and related life sciences domains.
Nextrove serves clients across pharmacovigilance, hosting, artificial intelligence solutions, eTMF, RIM, regulatory affairs, clinical operations, medical information, Salesforce, and integration services. The company's business experts have held leadership roles in pharmaceutical, biotechnology, and CRO organizations, and its technology leaders have experience implementing safety systems. Nextrove also offers deployable frameworks and accelerators intended to support efficient project delivery.
Services
- Argus Safety Implementation, Upgrade & Migration: Provides comprehensive Argus Safety solutions tailored to pharmacovigilance needs, covering implementation, system upgrades, and data migration.
- LSMV Implementation and Migration: Delivers end-to-end management, consulting, custom development, and managed services support for Life Sciences Master Vault (LSMV) products.
- Business Transformation: Supports business integration, business process redesign, systems assessment, and the development and implementation of solutions.
- NextCloud Hosting Solutions: Offers cloud-based hosting solutions designed for businesses of varying sizes.
- Managed Services: Provides 24/7 coverage to maintain safety systems and delivers resolution to updates and issues.
- Japan, China, Korea Dedicated Services: Offers both local and global support specifically for clients based in Japan, China, and South Korea.
Progressive Suite — Products
- Progressive Intake: Addresses adverse event and product complaint management in complex regulatory environments, designed to be robust, secure, flexible, and intelligent.
- Progressive Convey: Automates the distribution of safety documents to investigators globally.
- Progressive Compliance: Provides end-to-end support for managing Pharmacovigilance System Master File (PSMF) preparation and aggregate report preparation and submission, functioning as an intelligent assistant for safety teams.
- Progressive GFA (Global Follow-up Automation): Automates follow-up queries and questionnaire management to ensure precision and efficiency in case handling.
- Progressive GRT (Global Regulatory Triage): A solution designed to address the demands of complex regulatory environments through triage automation.
- GRRACE: A modular engine designed to optimize reporting rule maintenance within Argus Safety, using automation and customizable features to improve efficiency and accuracy.
- Progressive ClinConnect: Provides an advanced platform for bulk data import into the Argus Safety application, supporting efficient safety data management.
- Progressive MICC: An all-in-one solution for pharmaceutical companies designed to streamline contact center operations.
- Progressive Reporting & Analytics: A platform for analyzing safety data, used to create reports, dashboards, stories, and explorations.
- Progressive TransX: A translation and language tool supporting regulatory data, complex safety application data, and business communications across multiple languages.
Company Background and Presence
- Over 20 years of experience in life sciences professional services and technology implementation.
- Global office presence across the United States, United Kingdom, Italy, Japan, China, South Korea, and India.
- The Progressive Suite is in active use across numerous pharmaceutical, biotech, and CRO organizations.
- Participates in industry events including the Aris Global Breakthrough APAC summit, CMAC PV Annual Meeting in China, and BIO Korea.
- Has published case studies covering pharmacovigilance operations transformation, Argus Safety optimization, and FDA R3 compliance support.
- Areas of consulting coverage include pharmacovigilance, regulatory affairs, clinical operations, eTMF, RIM, medical information, Salesforce, and integration services.
Nextrove positions itself as a niche consulting and technology firm bridging business expertise and technical capability for life sciences organizations navigating regulatory compliance and digital transformation in pharmacovigilance and related functions.
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