A current SOP needs training materials.
Your team owns the procedure, but needs help turning it into a concise, reviewed learning module.
For clinical laboratory leaders
Bion Med helps clinical laboratories turn a current SOP into reviewed learning materials, or organize a confirmed records gap within the systems they already use.
Start with one site, one system and one named test or procedure.
Where we can help
The first conversation looks at your actual workflow and available tools. We identify whether a small project would be useful.
Your team owns the procedure, but needs help turning it into a concise, reviewed learning module.
You want clearer links between people, SOP versions, training completion and practical assessment evidence.
The software may already support the task. The need may be content production, configuration or a more usable handoff.
Two ways to start
Route A · Records workflow
For a confirmed gap in record organization, dates or retrieval.
Route B · SOP training + handoff
For a laboratory that needs help producing and handing over its own procedure-based content.
The first scope covers one site, one system, one named test or procedure and up to ten testing personnel. Route B uses the agreed records workflow; a full Route A implementation is quoted separately if needed.
How it works
Your team approves the technical content and the operating rules. Bion Med manages the contracted production and documentation work.
A free 30-minute call about one process, your systems and the task you want to improve.
A short written workflow map, followed by a scoped proposal when a project is useful.
Produce the selected route with a named laboratory reviewer and consolidated feedback.
Check the agreed output, obtain written acceptance and hand over the contracted assets and instructions.
Clear ownership
The agreed project supports your existing quality process. Your laboratory retains technical approval, practical competency assessment and staff authorization.
The contracted learning materials, record structure, handoff and operating instructions.
SOP accuracy, assessor eligibility, practical assessment results, applicable date rules and authorization to perform testing.
The service does not award accreditation, certify personnel competency or guarantee an inspection outcome.
Project lead
MD, MBA
Healthcare & diagnostics
Direct senior involvement
With more than 20 years in healthcare and diagnostics, Nenad led regional Roche Diagnostics and Diabetes activities at ADOC across Southeast Europe.
His laboratory collaborations include Synevo/Medicover, SYNLAB, individual laboratories across the region, and laboratories in public primary, secondary and tertiary healthcare institutions. These relationships began through ADOC and continued through Bion Med.
For this service, he is the named Bion Med contact for the workflow review and agreed project.
Before we speak
We first check the tools and workflow you already use. A new tracker is considered only when an agreed gap remains. Any import, export or integration is scoped and tested in your actual licensed environment.
One laboratory site, one named system, one named test or procedure, and up to ten testing personnel. The SOP route covers one SOP revision, a video of up to five minutes, 7–10 entry and 7–10 exit knowledge questions, and two consolidated review rounds. Additional sites, tests or modules are scoped separately.
Training completion and practical competency assessment are kept separate. Your laboratory selects qualified assessors, performs and evaluates the practical assessments, and decides staff authorization. Bion Med prepares the agreed content and documentation workflow.
Do not send SOP files, staff records or patient information through the public inquiry form. Before materials or access are shared, we agree the permitted data, tools, access and storage arrangements with your laboratory. Demonstrations use fictional data.
After the workflow conversation, you receive a written proposal defining the selected route, deliverables, fee, payment terms, review rounds and acceptance criteria. Delivery dates are agreed around complete inputs, approved access and laboratory review availability.
The contracted training or records materials, the agreed source or editable assets, instructions for the selected workflow, and a handover walkthrough. Your team checks the agreed output before accepting the work.
Yes. The fictional example shows how SOP training completion can be linked to a visible list of missing practical evidence. It contains no real laboratory or employee records and is not a client case study.
Start with one process
We will discuss how it works today, what your existing tools can do and whether a small, clearly scoped project would help.
Prefer email? contact@bion-med.com
Please do not send SOP files, staff records or patient information with your initial inquiry. Confidential materials and access are agreed separately.
You receive a short written workflow map after the call. Any proposed project has a separately agreed scope, fee, timeline and acceptance criteria.