Average Ratings 0 Ratings
Average Ratings 0 Ratings
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
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