Sterile compounding - Garbing and work in the hood
ConductVision can check garbing, hand hygiene and glove disinfection in your cleanroom suite and flag missed steps for a trained reviewer on your team.
Compounding in the cleanroom suite
Staff garb in the anteroom, then compound sterile preparations in the hood or isolator in the buffer room.
Your procedures set the garbing sequence, hand hygiene before gloving, when gloves are disinfected before going back into the hood and how many people may be in the buffer room.
What goes wrong in the cleanroom suite
- Someone skips a garbing step or does it out of sequence.
- Hand hygiene is skipped before gloving.
- Gloves go back into the hood without being disinfected.
- More people are in the buffer room than allowed.
What you get
Garbing on record
Each garbing step checked in sequence, with a short clip when one is missed.
Hand and glove checks
It flags skipped hand hygiene before gloving and gloves not disinfected before going back into the hood.
Decisions kept with the clip
A trained reviewer on your team confirms each event, dismisses it with a reason or escalates it to your designated person or QA. The audit trail keeps who decided, in what role, when and why.
Records for investigations
A record of each flagged event, to attach to an investigation, and a monthly report that one person reviews and a second person approves.
How a pilot works
Full recordings stay on your network. For each event it flags, ConductVision saves a record and a short clip at your site.
First look
We look at footage you choose to share with us and agree with your team on what to watch for.
Paid pilot
ConductVision connects to your camera system and runs for a set time.
Pilot results report
You get a report of the results on your own footage, checked against the criteria your team set.
Your decision
You decide whether to roll out, change the scope or stop.
One question to start with
Are gloves disinfected each time before going back into the hood?
More pages in this section
- Sterile drugs and biologicsFill-finish lines, RABS and isolators
- Cell and gene therapyOpen steps in biosafety cabinets
- Medical devicesAssembly and packaging cleanrooms
- Food and beverageAseptic processing and packaging
- Electronics and semiconductorsFab, assembly and test cleanrooms
- Spacecraft and satellitesFlight hardware cleanrooms
- Cleanroom gowningGowning rooms and gowning procedures
- EU GMP Annex 1Sites making sterile medicines for the EU