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  6. Ensuring the reliability of data in drug discovery research and quality control.

Ensuring the reliability of data in drug discovery research and quality control.

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last updated:Jun 18, 2026

モレキュラーデバイスジャパン 東京本社
モレキュラーデバイスジャパン 東京本社
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"SoftMax Pro GxP" - a plate reader control and analysis software that ensures the reliability of data related to drug discovery and quality control.

"SoftMax Pro GxP" is a highly secure software that is fully compliant with FDA 21 CFR Part 11, maintaining data integrity through a streamlined workflow. It is optimized to simplify various operations, from controlling the microplate reader of molecular devices to data acquisition, analysis, and report generation. 【Features】 ■ Track and Record All Changes The system's audit trail tracks and records all changes, including timestamps, usernames, user IDs, section statements, signature information, and measurement results. ■ Achieve Secure Document Sharing Document data is stored in a Microsoft SQL database, enabling thoroughly managed document sharing with controlled access permissions. ■ Maintain Data Integrity By using a paperless document status system, data integrity can be maintained through electronic signatures and document workflows. *For more details, please refer to the PDF materials or feel free to contact us.

    Software (middle, driver, security, etc.)
SoftMax+Pro+7.1.jpg

Ensuring the reliability of data in drug discovery research and quality control.

SoftMax+Pro+7.1.jpg
SoftMax+Pro+7.1.jpg
  • Related Link - https://www.moleculardevices.co.jp/products/microp…

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Free Seminar: Basic Requirements for CSV and Data Integrity and Inspection Response

Free Seminar: Basic Requirements for CSV and Data Integrity and Inspection Response

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Basic Knowledge of CSV, Roles of Users and Suppliers, Category Classification, Recent Developments in DI Guidance, Points to Consider in Contracted Operations, Considerations for Managing and Handling Electronic Data, Key Points for CSV and DI Inspections by Regulatory Authorities, Special Seminar with Clear Explanations Based on Extensive Experience!! ◆Instructor Kenichi Ogiwara, Representative of C-Cast Co., Ltd. Currently active after working at Yokogawa Electric Corporation and Nomura Research Institute. ◆Target Audience Individuals involved in CSV and Data Integrity at pharmaceutical companies, medical device manufacturers, suppliers, etc. ◆Prerequisites No specific prior knowledge required. ◆Knowledge to be Acquired 1) Basic knowledge of CSV 2) Role division between users and suppliers in CSV 3) Correct thinking about category classification 4) Recent status of data integrity guidance 5) Japanese authorities' perspective on data integrity 6) Points to consider in contracted operations (labs and manufacturing) 7) Considerations for managing and handling electronic data 8) Key points for inspections of CSV and data integrity by regulatory authorities.

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モレキュラーデバイスジャパン

モレキュラーデバイスジャパン 東京本社

Research and development equipment and devices

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Molecular Devices Japan, Inc. is a leading global provider of high-performance bioanalytical measurement systems, software, and consumables for life science research, drug development, and biotherapeutics, including microplate readers and imaging systems. We are committed to the continuous development of innovative solutions for life science applications.

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