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Average Ratings 0 Ratings

Total
ease
features
design
support

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Write a Review

Description

Laboratory information management systems are crucial for accurately documenting and protecting the origin and characteristics of a product batch. The significance of this information is greatly amplified when it is captured and managed throughout the complete trade cycle. Additional data collected during this process can be utilized and tracked across the whole value chain, promoting greater transparency. These systems record a diverse range of both standard and custom product attributes, such as moisture content measurement, bean count and cut, color, aroma, shape, roast level, staple length, and weight per unit of volume. Users have the flexibility to define additional specifications according to their unique requirements, which are seamlessly integrated into the ongoing data collection process and trade lifecycle. Depending on the specific commodity and quality control measures in place, visual assessments of defects and size counts will be documented for each unit. Furthermore, physical profiling can extend to include evaluations of color and shape grading, ensuring comprehensive quality assessment. This level of detail not only enhances product quality assurance but also fosters trust among stakeholders in the supply chain.

Description

The General NCMR search form is utilized to find NCMRs based on user-defined criteria. This search tool is consistent across all NCMR-related icons, so we will examine the search interface in detail. To access this interface, simply click on the General NCMR Search icon located in the main QCS9000 navigator. Supplier NCMRs are typically generated during the incoming inspection phase and relate to defects in materials sourced from external vendors. In-Process NCMRs arise from defects detected during the manufacturing process or when products are moved between work centers, often identified through quality control inspections. Customer Return NCMRs occur when clients return shipped items due to identified defects or nonconformities. Additionally, terms like RMA (Returned Material Authorizations) and CRM (Customer Return Material) are often associated with these processes. Understanding these categories is crucial for managing quality assurance effectively and ensuring that products meet the required standards before reaching customers.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

Infor CRM Yes 
Microsoft Dynamics 365 Yes 
SAP Cloud Platform Yes 

Integrations

Infor CRM No 
Microsoft Dynamics 365 No 
SAP Cloud Platform No 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

$995 per month
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 No 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows Yes 
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 No 
Live Training (Online) No 
In Person Yes 

Types of Training

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

Vendor Details

Company Name

PCR

Founded

2019

Country

United Kingdom

Website

pcruk.com/cc1-lab-%26-quality

Vendor Details

Company Name

JK Technologies

Website

www.jkt9000.com

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 

LIMS

Audit Trail No 
Certificates of Analysis No 
Data Import / Export No 
Electronic Laboratory Notebook No 
Inventory Management No 
Lab Instrument Interface No 
Reporting & Statistics No 
Sample Tracking No 
Specification Management No 
Workflow Management No 

Product Features

Quality Management

Audit Management No 
Complaint Management Yes 
Compliance Management Yes 
Corrective and Preventive Actions (CAPA) Yes 
Defect Tracking Yes 
Document Control Yes 
Equipment Management Yes 
ISO Standards Management No 
Maintenance Management No 
Risk Management No 
Supplier Quality Control No 
Training Management No 

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