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LT-Connect 5.8 (Literature Information Monitoring and Evaluation)

Quickly evaluate and report safety information obtained from literature and conference data in a paperless manner!

LT-Connect is a solution focused on the collection and evaluation of literature information, which is one of the safety measures in pharmaceutical operations. It screens literature information obtained from SDI service companies (primary evaluation, etc.), and if additional information is needed for secondary evaluation or if a detailed investigation is required, this function allows for investigation requests to be sent to Medical Representatives (MRs). MRs can receive requests and respond with investigation results using smartphones or iPads. The Pharmacovigilance (PV) department collects investigation results in a timely manner and determines the necessity of research reports (secondary evaluation, etc.). Additionally, if there are events that should be processed as individual reports based on literature information or detailed investigation results, they are handled as individual reports of adverse effects. This function retains all obtained literature information, screening and evaluation results, and records of MR activities related to literature information investigations, and it can share information with safety information management systems (such as Argus, ARIS, Persiv, etc.) for information that needs to be reported to regulatory authorities. It also centrally manages the collected literature information (SDI) along with PDFs.

Related Link - https://www.d-sols.com/products/connect-series/lt-…

basic information

**Features** - It allows for the bulk import of electronic data (CSV format) from SDI services such as JAPIC, WIMDIS, and IMIC. You can set the import information fields for each SDI service. - Not only bibliographic information but also original literature (in PDF format, etc.) can be managed with LT-C. Individual case information is managed in conjunction with AE-Connect. - If reporting to authorities is required based on the collected information, it can be managed in conjunction with a safety information database that supports industry standard formats (E2B compliant) for bulk import. - When evaluating literature information, processing flows can be set according to roles such as verification and approval. Each responsible person can smoothly carry out tasks according to their roles. - It can manage the activity status of literature research monitoring. - It imports obtained literature, conference information, and originals (PDF) for centralized management along with activity records. - It retains activity records of literature and conference information collection, investigation, and evaluation, as well as audit trails of registered information to ensure compliance with laws and regulations. - It can be implemented with validation support. (Validation services are available.)

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Model number/Brand name

Literature Monitoring and Evaluation System

Applications/Examples of results

It is being used by a major pharmaceutical company. *For more details, please download the PDF or feel free to contact us.*

Detailed information

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