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Average Ratings 0 Ratings

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ease
features
design
support

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Description

To protect sensitive information, including personally identifiable information (PII), organizations must implement techniques such as pseudonymization and anonymization for secondary purposes like comparative effectiveness studies, policy evaluations, and research in life sciences. This process is essential as businesses amass vast quantities of data to detect patterns, understand customer behavior, and foster innovation. Compliance with regulations like HIPAA and GDPR mandates the de-identification of data; however, the difficulty lies in the fact that many de-identification tools prioritize the removal of personal identifiers, often complicating subsequent data usage. By transforming PII into forms that cannot be traced back to individuals, employing data anonymization and pseudonymization strategies becomes crucial for maintaining privacy while enabling robust analysis. Effectively utilizing these methods allows for the examination of extensive datasets without infringing on privacy laws, ensuring that insights can be gathered responsibly. Selecting appropriate de-identification techniques and privacy models from a wide range of data security and statistical practices is key to achieving effective data usage.

Description

Assign a distinctive identification number to each specimen while gathering pertinent clinical information. Organize specimens according to participants, protocols, departments, investigators, institutions, disease sites, anatomical locations, and other relevant categories. Segment samples into new specimens that receive new unique IDs along with their corresponding data. Ensure the tracking of each specimen from the point of collection through freezing, thawing, and eventual disposal. Maintain compliance with HIPAA regulations, allowing for data de-identification where necessary. Oversee various biospecimen repositories simultaneously. Collect specimens in accordance with protocol calendar timepoints or through a single event timepoint, as required. Additionally, keep track of and upload consent forms and other necessary documents. Create a freezer and storage container configuration that accurately reflects physical storage conditions. Generate multiple customizable reports for inventory management, quality assurance, consent documentation, manifest creation and tracking, invoice management, and more. The system should allow users to efficiently query the specimen repository for specific types of samples, enhancing usability and accessibility. Furthermore, ensure that all data is accurately recorded and easily retrievable to facilitate ongoing research and analysis.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

No details available.

Integrations

No details available.

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

$14,500 per year
Free Trial No 
Free Version No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person Yes 

Types of Training

Training Docs No 
Webinars No 
Live Training (Online) No 
In Person No 

Vendor Details

Company Name

Fasoo

Country

United States

Website

en.fasoo.com/products/analyticdid/

Vendor Details

Company Name

DDOTS

Founded

1994

Country

United States

Website

www.ddots.com/biospec/

Product Features

Product Features

Lab Inventory Management

Barcode Scanning No 
Expiration Date Management No 
Purchasing No 
Reorder Management No 
Sample Management No 
Supply Management No 
Usage Tracking No 
Vendor Management No 

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