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WEBINAR | Medical Devices: Regulations and Chemical Characterization

Dr. Andrew Feilden shares key insights into the medical device regulatory landscape and discusses key aspects of extractable and leachable analysis requirements associated with newly revised ISO 10993-18.

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How-to シリーズ

Currently loaded videos are 1 through 15 of 96 total videos.

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11:23
Building a Toxicology Screening Processing Method: Part 2: Creating filters
Building a Toxicology Screening Processing Method: Part 2: Creating filters
7:52
Building a Toxicology Screening Processing Method: Part 1: Creating a workflow
Building a Toxicology Screening Processing Method: Part 1: Creating a workflow
13:42
Overview of OligoWorks SPE Workflow
Overview of OligoWorks SPE Workflow
11:14
Grant Application Support for Instrument Funding
Grant Application Support for Instrument Funding
10:34
MassLynx Skyline Interface (MSI) Tool
MassLynx Skyline Interface (MSI) Tool
11:02
How-to-Series Episode 4: How to Improve Performance of LC-MS/MS Analyses
How-to-Series Episode 4: How to Improve Performance of LC-MS/MS Analyses
12:41
How-to-Series Episode 3: Assess and compensate for the effect of matrix on LC-MS/MS analyses
How-to-Series Episode 3: Assess and compensate for the effect of matrix on LC-MS/MS analyses
2:53
Replacing the Solvent Filters
Replacing the Solvent Filters
7:35
Ramp Test to Monitor Check Valve Performance
Ramp Test to Monitor Check Valve Performance
1:58
Priming and Purging the 1525 Binary HPLC Pump
Priming and Purging the 1525 Binary HPLC Pump
8:42
Replacing the Plunger Seal and Plunger
Replacing the Plunger Seal and Plunger
3:36
Replacing a Check Valve Cartridge
Replacing a Check Valve Cartridge
5:26
Performing the Ramp and Decay Test After a PM
Performing the Ramp and Decay Test After a PM
7:30
Rebuilding the Reference Valve
Rebuilding the Reference Valve
12:12
How-to-Series Episode 2: Prepare Biological Samples for LC/MS/MS Analysis
How-to-Series Episode 2: Prepare Biological Samples for LC/MS/MS Analysis

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