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Tom Cruise Couldn’t Even Steal Your Material: Technology to Protect Your Files

Those of you who've seen the "Mission Impossible" movie franchise know they often make the impossible seem all too plausible.

Getting Published - How Important is a Peer Review?

If you're new to your scientific industry, it's time to learn an important part of what helps you gain more sponsors based on your research clout.

The Clear Benefits of Outsourcing Your IHC Histopathology

Are you planning on performing IHC as part of your study? Is the data you obtain from IHC critical in your decision making process? As any scientist knows, it is very important to plan your experiment well to achieve high-quality, repeatable results.

Fixation 101: A Primer for Outsourcing Your Histopathology

Clearly, experimental tissue samples are vital to any study. Before you sacrifice your animal or start preparing buffers, here are a few fundamental techniques and practices that will help you excise an ideal sample before sending those samples to us for further histopathological assessment.

The Importance of Consistent Slide Production from Study to Study

Creating slides in your histology lab might seem routine, though your reputation rests solely on the results.

Why should I use a GLP Lab when my study is non-GLP?

Adhering to Good Laboratory Practices (or GLP) should become a routine aspect in the histology industry.

4 Benefits of Outsourcing Your IHC Histopathology

As any scientist knows, a lot can go wrong during an experiment. Once you have your final samples and you’re ready for analysis, that’s not the time to be taking any chances.

3 Reasons Why Organizations are Outsourcing Their Histopathology

Businesses and organizations have similar reasons for outsourcing non-core functions, yet some functions are more crucial than others.

Four Reasons to Store Your Research at an Archiving Facility

Running a histology lab is going to involve a lot of research material that could easily become damaged if you're running out of space.

The Importance of Preclinical Research Under the FDA Animal Rule

When the FDA Animal Rule, or Animal Efficacy Rule, became law in 2002, it created a pathway for assessing the safety and efficacy of drugs and biological products for “serious or life-threatening conditions caused by exposure to lethal or permanently disabling substances” when human clinical trials are not ethical or feasible.

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