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Platform and Features

Read more about our core features and platform capabilities

LIMS
Essential data management, tracking, and workflows for compliant pharmaceutical organizations

ELN
Laboratory data management, security, collaboration, compliance, and efficiency

Sample Management
Maintain the integrity, traceability, and accuracy of laboratory samples

Inventory Management
Manage chemical inventory and maintain the integrity, traceability, and accuracy of end results

Equipment Management
Ensure a complete record of equipment events and a usage log of where and when the equipment was used

Read more:

Our most commonly queried extra core features are below.
Looking for something else? See our full list of core features here.

Solutions

Looking for something more specific? Read through the other solutions we support out of the box

Batch Records
Utilize Batch Records to prevent errors and negative impacts to the final product

Environmental Monitoring
Unify and simplify your environmental monitoring workflows by centralizing data management

Stability
Reliably manage your stability programs, reducing errors, and providing a toolset for effective stability testing, analysis, and reporting

Next Generation Sequencing
Ensure secure management and tracking of NGS samples from extraction to data analysis

Chromatography
Expose your chromatography data across your organization to improve decision making

Mass Spec
Elevate efficiency, assure compliance, and streamline your Mass Spec information process

Inhalation
Complete modules for Inhaled development

Formulation
Implement a flexible common framework for recording formulation experiments across the organization

Resources

Browse our archive case studies, functional documentation, and announcements.

Looking for something specific? Search our site:

See case studies on implementations our customers have used to achieve specific outcomes:

Compliance Case Study
Compliance is at the core of our platform, ensuring adherence to GxP regulations and guidelines.

Spreadsheets Case Study
Use our unique spreadsheet paradigm to eliminate the need for code in your solution configuration

Comprehensive Case Study
Document all phases from development to manufacturing in one platform

Other Resources:

Frequently used or consulted tools and information

Our Documentation:

Search these pages for a wider variety of documentation

Validated Spreadsheet Strategy

Spreadsheets are often the best solution for scientists to document laboratory processes and generate data. As a result, if not validated and utilized in the appropriate manner, spreadsheets can quickly proliferate with a negative impact on data management and compliance .

SciCord supports your continued use of spreadsheets, adding life-cycle and compliance features to enhance security and control of your data.

Spreadsheets in SciCord
Document Lifecycle
Compliance

Spreadsheets in SciCord

SciCord implements a spreadsheet paradigm so you retain your familiar spreadsheet interface
Import existing spreadsheets into SciCord for complete version control and security
Imported spreadsheets are immediately ready for use and are fully compliant with 21 CFR Part 11 including electronic signatures and audit trail
Spreadsheets can be enhanced with additional functionality unique to SciCord, such as sample management, resources, label printing, result extraction, etc.

Documents can progress through the system over time in several ways, depending on the level of accountability needed.

Document Lifecycle

A document in SciCord is synonymous with notebook or experiment.
Each document is subject to a managed/controlled lifecycle.
The steps of the lifecycle are defined based on the compliance required for the document content.

Compliance

SciCord ELN/LIMS is designed for laboratory and manufacture compliance. Improve your compliance using locked validated formulas to eliminate calculation errors.
Defined lists to assure adherence to SOPs.
Automatic entry verification to flag potential Out-Of-Specification situations.
Restrictions to avoid use of expired solutions or assure use of equipment by trained individuals.
Intelligent scans alert reviewers of potential issues with precision, unstable balance, uncalibrated equipment, un-validated process.
Fully compliant with CFR 21 Part11 including electronic signatures and audit trails.

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