FEATURED EDITORIAL
Cleaning Process Capability: Risk-Based Cleaning Process Performance Qualification
By Andrew Walsh et al.
A cleaning validation professional must know how many process performance qualification runs are necessary. Here's how to go about demonstrating this with a high degree of assurance while minimizing the number of qualification runs.
Considerations For Rapid Prototyping In Medical Device Development
By Jim Kasic, Boulder iQ
Rapid prototyping has taken the medical device industry by storm, but there are pros and cons that device developers need to consider.
INDUSTRY INSIGHTS
Regulatory Compliance For Prefilled Syringes And Auto-Injectors
Eurofins
The Science And Engineering Of Advanced MRI Machines
By Peter Matthews, Knowles Precision Devices DLI
Material Selection With An Eye On Micro-Molding
Accumold
"Is It On Yet?" - Silent Operation With Disc Pump
The Lee Company
TIRF Microscopy Using Super-Resolution Microscopy Cubes
IDEX Health & Science, LLC
Comparing “Apples To Apples” With Your Med Device Injection Molding RFQ's
Medbio
Introducing High-Q Ceramic Core Inductors
Knowles Precision Devices DLI
Improve Speed To Market By Mitigating Vial And Stopper Incompatibility
By Victoria Morgan, West Pharmaceutical Services, Inc.
Reducing Risks In Your SIP Validation Cycles
Mesa Laboratories
Outset Medical: A Digital Transformation Success Story
Tulip
