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BarTender Software
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Allergen Labelling
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Freight Labelling - SSCC
RFID
SSCC and Cross Dock Labelling Solution
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Cybake
Epicor
ERP, WMS, MES
IBM Websphere
Infor
JD Edwards
Körber
Microsoft Business Central
Microsoft Dynamics
MYOB
NetSuite
ORACLE
Pronto
riteSOFT and riteSCAN
SAGE
SAP
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Weighing Scales
Regulations & Standards
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Allergen (PEAL - Plain English Allergen Labelling)
Food Nutrition and Beverage
Country of Origin Labelling (CoOL)
GS1
GHS (Labelling of Chemicals)
CLP (Chemical Substances and Mixtures)
EU MDR (Medical Device Regulation)
FDA UDI (Unique Device Identification)
EU GMP Annex 11 (Medical Device and Life Science)
FDA 21 CFR Part 11 - Clinical Trial Labelling (Medical Device and Life Science)
FDA 21 CFR Part 312 - Electronic Records (Medical Device and Life Science)
Log in
Create account
Search
Contact
BarTender Software
Software Editions and Features
What's new in BarTender 2022 ?
BarTender Cloud
BarTender Cloud
Supplier Labelling
Buy
BarTender On-premise Software
Compare Editions
- Starter
- Professional
- Automation
- Enterprise
BarTender Cloud
Compare Editions
- Cloud Essentials
- Cloud Automation
Maintenance and Support
- Standard
- Premium
Professional Services
Updates and Upgrades
Free Trial
BarTender On-premise Software
BarTender Cloud
Previous Versions
Support & Services
Get Support
End of Support and End of Sale Dates
Software Download - Previous Versions
Services
Useful Links
Solutions
Allergen Labelling
Amazon Transparency Program
Case Studies and Videos
Chemical Labelling
Country of Origin Labelling (CoOL)
Food and Beverage
Freight Labelling - SSCC
RFID
SSCC and Cross Dock Labelling Solution
Supplier Labelling
Integrations
Cybake
Epicor
ERP, WMS, MES
IBM Websphere
Infor
JD Edwards
Körber
Microsoft Business Central
Microsoft Dynamics
MYOB
NetSuite
ORACLE
Pronto
riteSOFT and riteSCAN
SAGE
SAP
SYSPRO
Weighing Scales
Regulations & Standards
Allergen (PEAL - Plain English Allergen Labelling)
Food Nutrition and Beverage
Country of Origin Labelling (CoOL)
GS1
GHS (Labelling of Chemicals)
CLP (Chemical Substances and Mixtures)
EU MDR (Medical Device Regulation)
FDA UDI (Unique Device Identification)
EU GMP Annex 11 (Medical Device and Life Science)
FDA 21 CFR Part 11 - Clinical Trial Labelling (Medical Device and Life Science)
FDA 21 CFR Part 312 - Electronic Records (Medical Device and Life Science)
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