Plauti
Plauti is a data quality platform built natively for CRM, designed for organizations that want tight governance, strong security, and practical control over the accuracy of their customer data. Unlike solutions that move data to external servers or require separate platforms, Plauti runs entirely inside your existing CRM infrastructure, so no data leaves your system and no additional security perimeter is introduced.
For Salesforce customers, Plauti covers the end-to-end data quality lifecycle:
Prevent duplicates at the source: Real-time alerts notify users of potential duplicates as they enter records, helping sales, marketing, and service teams keep data clean from the start.
Protect against hidden duplicates: Detect duplicates created by imports, integrations, and APIs to keep inbound data streams aligned with your standards.
Remediate at scale with batch jobs: Run configurable batch processes to find, review, and merge existing duplicates across large data volumes, with full audit trails that support compliance, internal controls, and reporting.
Verify contact information: Check email addresses and phone numbers before they’re saved to reduce bounce rates, improve campaign performance, and support more reliable outreach.
All of this operates on Salesforce’s own infrastructure, using your existing permissions, roles, and security model. There is no separate user login, no data sync lag to manage, and no additional compliance gap to justify to auditors or security teams.
For Microsoft Dynamics 365, Plauti focuses on robust duplicate prevention and control. Admins can configure real-time alerts, leverage API-based detection, run batch processes, and apply cross-entity matching rules to keep accounts, contacts, and leads aligned and consolidated.
Plauti is built for CRM admins, data stewards, and operations teams who need immediate, self-service control over data quality—without waiting for developers, complex projects, or long IT ticket queues.
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DataBuck
Ensuring the integrity of Big Data Quality is crucial for maintaining data that is secure, precise, and comprehensive. As data transitions across various IT infrastructures or is housed within Data Lakes, it faces significant challenges in reliability. The primary Big Data issues include: (i) Unidentified inaccuracies in the incoming data, (ii) the desynchronization of multiple data sources over time, (iii) unanticipated structural changes to data in downstream operations, and (iv) the complications arising from diverse IT platforms like Hadoop, Data Warehouses, and Cloud systems. When data shifts between these systems, such as moving from a Data Warehouse to a Hadoop ecosystem, NoSQL database, or Cloud services, it can encounter unforeseen problems. Additionally, data may fluctuate unexpectedly due to ineffective processes, haphazard data governance, poor storage solutions, and a lack of oversight regarding certain data sources, particularly those from external vendors. To address these challenges, DataBuck serves as an autonomous, self-learning validation and data matching tool specifically designed for Big Data Quality. By utilizing advanced algorithms, DataBuck enhances the verification process, ensuring a higher level of data trustworthiness and reliability throughout its lifecycle.
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PubMed
PubMed® serves as a vast database with over 35 million citations pertaining to biomedical literature, which is derived from MEDLINE, various life science journals, and an array of online books. Numerous citations offer access to full-text articles, which can be found via PubMed Central and the publishers' websites. This critical resource aims to streamline the process of searching and retrieving literature in the biomedical and life sciences sectors, ultimately striving to improve health outcomes on both global and individual scales. While the PubMed platform does not include full-text journal articles directly, it frequently provides hyperlinks to these articles when available from other sources, such as the publisher's website or PubMed Central (PMC). The citations featured in PubMed primarily stem from areas related to biomedicine and health, along with interrelated fields including life sciences, behavioral sciences, chemical sciences, and bioengineering. A considerable portion of PubMed comprises MEDLINE, which includes citations from journals that have been selectively chosen for this collection. Researchers, healthcare professionals, and those interested in medical advancements regularly turn to this platform to remain updated on the newest research findings and developments in the medical field, ensuring they have access to the most relevant information. As such, PubMed stands as an essential tool in the pursuit of improved health knowledge and practices.
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Drug Safety Triager
Clarivate's Drug Safety Triager is a sophisticated pharmacovigilance solution designed to assist life sciences organizations in meeting regulatory requirements effectively. This tool, which has been validated for Good Practice (GxP) compliance and is ready for audit processes, optimizes the workflow involved in literature reviews, enabling pharmacovigilance experts to focus on patient safety by refining these actions. Fully aligned with the reporting requirements of leading global safety regulatory authorities such as the FDA and EMA, the Drug Safety Triager is accompanied by a thorough validation package with each implementation. The validation documentation is meticulously crafted to satisfy the rigorous standards established by the pharmaceutical industry and health governing bodies. Moreover, every literature item included undergoes a detailed review, ensuring that all user interactions are meticulously documented, thus creating a permanent, unalterable audit trail that promotes accountability and transparency. This forward-thinking approach not only boosts operational efficiency but also reinforces the unwavering dedication to upholding high standards in patient safety and compliance with regulations. Ultimately, the Drug Safety Triager represents a pivotal advancement for organizations striving to enhance their pharmacovigilance practices while ensuring robust safety and regulatory adherence.
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