Applications from the field of Pharma & Biopharma | LabRulez GCMS

Demonstrating Inertness for the Analysis of Nucleotides on the Agilent 1290 Infinity II Bio LC

Technical notes

| 2022 | Agilent Technologies

HPLC

Instrumentation

HPLC

Manufacturer

Agilent Technologies

Industries

Pharma & Biopharma

Analysis of Peptide/Protein*-Related Impurities Using the Integrated Solution of Bio 2D-LC/Q-TOF in Agilent MassHunter Software

Technical notes

| 2022 | Agilent Technologies

LC/TOF, LC/HRMS, LC/MS, LC/MS/MS, 2D-LC

Instrumentation

LC/TOF, LC/HRMS, LC/MS, LC/MS/MS, 2D-LC

Manufacturer

Agilent Technologies

Industries

Pharma & Biopharma

Using Chromeleon 7 Chromatography Data System to Comply with 21 CFR Part 11

Technical notes

| 2018 | Thermo Fisher Scientific

Software

Instrumentation

Software

Manufacturer

Thermo Fisher Scientific

Industries

Pharma & Biopharma

Demystifying Software Validation: Learn What Software Validation Means for You and Your Lab

Technical notes

| 2017 | Agilent Technologies

Software

Instrumentation

Software

Manufacturer

Agilent Technologies

Industries

Pharma & Biopharma

Data Integrity in Pharmaceutical Quality Control Laboratories: What You Need to Know

Technical notes

| 2016 | Agilent Technologies

Software

Instrumentation

Software

Manufacturer

Agilent Technologies

Industries

Pharma & Biopharma

Evaluating BioAccord System Performance in Late Stage Development and QC Environment – Peptide Mapping Analysis

Technical notes

| 2020 | Waters

LC/TOF, LC/HRMS, LC/MS

Instrumentation

LC/TOF, LC/HRMS, LC/MS

Manufacturer

Waters

Industries

Pharma & Biopharma

Automating the Creation of Chromatographic Methods for Method Validation Using Empower Sample Set Generator

Technical notes

| 2014 | Waters

Software, HPLC

Instrumentation

Software, HPLC

Manufacturer

Waters

Industries

Pharma & Biopharma

FUTURE-PROOF SOLUTIONS FOR REGULATED LABORATORIES IN THE FACE OF CHANGING USP <621> GUIDELINES

Technical notes

| 2015 | Waters

HPLC

Instrumentation

HPLC

Manufacturer

Waters

Industries

Pharma & Biopharma

Benefits of Using Mass Detection for Pharmaceutical Raw Materials Analysis of 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Hydrochloride

Technical notes

| 2015 | Waters

LC/MS, LC/SQ

Instrumentation

LC/MS, LC/SQ

Manufacturer

Waters

Industries

Pharma & Biopharma

Routine MS Detection for USP Chromatographic Methods

Technical notes

| 2015 | Waters

LC/MS, 2D-LC, LC/SQ

Instrumentation

LC/MS, 2D-LC, LC/SQ

Manufacturer

Waters

Industries

Pharma & Biopharma

Applications from the field of Pharma & Biopharma | LabRulez GCMS

Demonstrating Inertness for the Analysis of Nucleotides on the Agilent 1290 Infinity II Bio LC

Analysis of Peptide/Protein*-Related Impurities Using the Integrated Solution of Bio 2D-LC/Q-TOF in Agilent MassHunter Software

Using Chromeleon 7 Chromatography Data System to Comply with 21 CFR Part 11

Demystifying Software Validation: Learn What Software Validation Means for You and Your Lab

Data Integrity in Pharmaceutical Quality Control Laboratories: What You Need to Know

Evaluating BioAccord System Performance in Late Stage Development and QC Environment – Peptide Mapping Analysis

Automating the Creation of Chromatographic Methods for Method Validation Using Empower Sample Set Generator

FUTURE-PROOF SOLUTIONS FOR REGULATED LABORATORIES IN THE FACE OF CHANGING USP <621> GUIDELINES

Benefits of Using Mass Detection for Pharmaceutical Raw Materials Analysis of 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Hydrochloride

Routine MS Detection for USP Chromatographic Methods

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