Experience Unified Enterprise Command Across R&D and Quality
Life Sciences organizations are challenged by fragmented R&D and quality landscapes that reduce visibility, slow decisions and dilute the value of digital investments. At the Veeva R&D and Quality Summit, we’ll share how to create a unified enterprise command center by connecting data, processes and intelligence across your R&D ecosystem.
We bring deep R&D and quality expertise, paired with strong Veeva, digital engineering, data and advanced AI capabilities. We design scalable, Veeva-aligned architectures that integrate research, clinical, regulatory, safety and quality data—delivering governed interoperability and end-to-end transparency across the product lifecycle.
We embed responsible, scalable AI through advanced analytics and knowledge graphs directly into Veeva Vault workflows. This delivers predictive insights, automated, harmonized processes and real-time portfolio and compliance oversight without compromising data integrity or inspection readiness. Join us in Copenhagen at the Veeva R&D and Quality Summit 2026 to see how we help organizations operationalize AI-driven intelligence and modernize regulated landscapes with confidence.
Focus Areas
Our Capabilities
Users supported
Business users trained
Presence in countries
Life sciences clients
Our Solutions
AI-led patient recruitment
Gain a unified, comprehensive view of patient data across clinical, genomic and lifestyle information. By integrating and analyzing this data in real time, AI systems can intelligently match patients to suitable clinical trials, significantly reducing manual effort and accelerating recruitment timelines
AI-led data review optimization
Streamline clinical data cleaning, review and decision-making across the study lifecycle with an AI-augmented, risk-based data review framework. Establish an integrated RBIDR (risk-based integrated data review) operating model spanning clinical data management, monitoring, medical review and quality oversight.
Intelligent study design
Automate study design and simulation using integrated clinical data from solutions like Veeva Clinical, AI models and scenario testing. Optimize protocols, predict feasibility, reduce risk, accelerate timelines, control costs and enable data-driven decisions before study startup across therapeutic areas and trial execution planning.
Lab of the future
Adopt a comprehensive and flexible framework for laboratory digitization. We deliver an enterprise level digitization blueprint, end to end equipment connectivity, automated data flow and a centralized lab portal for operations. This maximizes business value from laboratory operations and elevates the end user experience.
Intelligent regulatory platform
Transform regulatory workflows with GenAI and Agentic AI across intelligence, planning, authoring, submissions and approvals. Improve compliance, accelerate time‑to‑submission, reduce manual effort and risk, enhance regulatory transparency and enable faster, data‑driven regulatory decisions at scale
Integrated safety platform
Unify safety operations with an end-to-end connected platform for AI-led use cases across automated intake and triage to translation and ICSR narrative creation across the pharmacovigilance lifecycle. Benefit from continuous monitoring and summarization of literature and real-world data. Includes intelligent assistants for risk management plans, periodic safety update reports and health authority responses.
Integrated compliance, validation and quality platform
Deploy an AI-intrinsic solution across CSV/CSA, testing, documentation and audit readiness. Achieve first‑time‑right validation, continuous compliance, predictive quality insights and faster inspections across regulated R&D, clinical, lab and manufacturing ecosystems, all with globally secure enterprise deployments
Our Team at Veeva R&D and Quality Summit 2026
Our team brings deep expertise across life sciences, Veeva platforms, data, AI and regulated operations. We work closely with clients to co-create solutions that address complex R&D and quality challenges while delivering measurable business outcomes.
Practice Head
LS Commercial and Veeva CoE
HCLTech
Client Partner
Life Sciences
HCLTech
Client Partner
Life Sciences
HCLTech
Practice Head
Pharmacovigilance/Safety
HCLTech
Success Stories
A leading American medical company successfully migrated vast amounts of documents and data with zero errors.
HCLTech modernized Veeva CRM to enhance customer engagement, streamline operations and ensure seamless adoption across global markets, driving significant operational efficiencies.
HCLTech defined a unified platform program for a Danish pharma enterprise
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