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PAGE1

Booth no. F31
Exhibition
|KOREA LIFE SCIENCE
Country
| Korea, South
Address
|12 Bongeunsa-ro 114-gil, Gangnam-gu, Seoul, Republic of Korea
Tel
|+82-10-5670-5994
E-mail
| hanjs@page1.co.kr
Exhibits
| GxP Solution
Company Type
| etc(IT솔루션기업)

Exhibitor Information

PAGE1 Co., Ltd., founded in 2015, is a digital healthcare IT company specializing in GxP solutions and consulting for the pharmaceutical, biotech, food, and cosmetics industries.
With seasoned practitioners deeply experienced in regulatory compliance, PAGE1 designs and delivers integrated GxP platforms ? EDMS, LIMS, QMS, LMS, and POP ? ensuring end-to-end data integrity and traceability.
Built on a cloud-based SaaS platform, PAGE1 provides low TCO, free upgrades, and full support for compliance with FDA and EU-GMP standards.

Individual Exhibit/Technology Introduction (Detailed)

  • Product Name : BQUBE EDMS
    BQUBE EDMS manages the complete lifecycle of GMP documents ? from creation and approval to distribution and disposal ? through structured workflows that ensure consistency and traceability. Its unified platform seamlessly integrates EDMS, QMS, and LMS in a single system, minimizing human error and ensuring data integrity. With built-in audit trail and paperless capabilities, BQUBE fully supports compliance with FDA and EU-GMP standards.
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  • Product Name : LIMSpro
    PAGE1 LIMS Pro is a Laboratory Information Management System designed for GMP and GLP environments, seamlessly integrating data across raw materials, products, instruments, and test methods. It minimizes manual input errors through automated instrument connectivity (LAS) and scientific data acquisition (SDMS). Standardized workflows manage the entire process ? from test request to result entry, review, approval, and release ? ensuring full compliance with FDA 21 CFR Part 11 and GMP/GLP requirements.
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  • Product Name : ELNpro
    PAGE1 ELNpro is an Electronic Lab Notebook (ELN) solution that standardizes and digitalizes research workflows to enhance productivity and data reliability. It replaces paper-based notebooks with permanent electronic records, automates repetitive tasks through workflows and templates, and ensures legal validity and Data Integrity via timestamping and Audit Trail. The system is fully compliant with FDA 21 CFR Part 11 and CSV requirements. ELNpro covers the full research lifecycle ? from notebook creation, review, and approval to material management, instrument control, test requests, and stability testing. Seamless integration with analytical instruments via SDMS and LAS enables real-time data collection, while an intuitive dashboard delivers instant visibility into research status.
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