What human intervention and sample preparation is needed in order to operate BioVigilant’s IMD instruments?
Related Questions
- What is the chance that two or more separate microbes will pass through BioVigilant’s IMD instruments so closely together that they may inaccurately be counted as one larger particulate?
- In what ways are BioVigilant’s IMD instruments preferred to conventional plate culturing methods and "rapid methods"?
- Are there any recent technical advances that have made it possible for BioVigilant to create IMD instruments?
