Digitalization of Battery Production

The Future of Battery Production

Delve into the transformative era of battery manufacturing, emphasizing sustainability, quality cont...

Digital Innovation in Battery Production

The Digital Leap in Battery Manufacturing

Discover the transformative journey toward digital excellence in battery manufacturing, emphasizing...

On Demand Webinar: The Digital Shift in Battery Manufacturing

On Demand Webinar: The Digital Shift in Battery Manufacturing

Explore the transformative impact of digital technology in battery manufacturing, delving into how i...

Data Integrity webinar

Webinar: Data Integrity

Watch this webinar to understand data integrity criteria and how to assess lab data management proce...

Power the Bench - An Enhanced Strategy for Data Integrity

Power the Bench - An Enhanced Strategy for Data Integrity

Achieve workflow control, traceability and data automation by integrating bench top instruments and...

Laboratory Data Management Guide

Laboratory Data
Management Guide

The Data Management Guide offers strategies for organizations that want to improve their lab data ma...

Laboratory Data Integrity Guide

Laboratory Data Integrity Guide

A knowledge collection on the ALCOA+ principle, SOP guidance, data management, and practical tips to...

21 CFR Part 11 Compliant Instruments

21 CFR Part 11 Compliant Instruments

Electronic Records on Instruments without a PC? Please read why experts state, that standalone instr...

Full compliance for 21 CFR part 11 and EU Annex 11

Full compliance for 21 CFR part 11 and EU Annex 11

Compliance for 21 CFR of FDA part 11 and EU Annex 11 regulations on electronic record submission is...

Why X-ray Inspection is Vital in Pharmaceutical Production | mt.com

5 Reasons You Should Use X-ray in Pharmaceuticals

In the highly regulated pharma sector, manufacturers can’t afford any adverse quality or safety issues. Discover how x-ray inspection can help.

Full compliance for 21 CFR part 11 and EU Annex 11

Full compliance for 21 CFR part 11 and EU Annex 11

Compliance for 21 CFR of FDA part 11 and EU Annex 11 regulations on electronic record submission is supported by LabX.

Digitalization of Battery Production

The Future of Battery Production

Delve into the transformative era of battery manufacturing, emphasizing sustainability, quality control, and the pivotal role of digitalization alongs...

HPLC weighing data transfer

Application Note: Automatic Data Transfer to Chromatography Software

Learn how automatic, error-free data transfer from balance to HPLC can improve your LC/GC workflow and help you meet FDA ALCOA+ regulatory requirement...

Biological Buffer Preparation Guide

Biological Buffer Preparation Guide

Improve productivity of buffer solution preparation by optimizing your workflow. Get tips and hints on weighing, pipetting and pH measurement.

Food Formulation Guide

Guide: Food Formulation

Learn more about weighing solutions for food formulation in the lab and production, as well as proven methods and tips to avoid errors.