Protocols, quality-control data and method reports
Documentation connects the research question to the methods, controls and quality checks, results and interpretation. It can support a laboratory handover, an investor presentation, a partnership discussion or work toward a regulatory submission. It should explain how an experiment was performed, what the data support and any relevant limitations.
What your project can include
The agreed package can include a protocol, QC information, a description of the analytical workflow and a scientific method report. For work performed by Biohagen, documentation can accompany assay development, molecular biology work or validation studies. If the documentation is for an external audience, tell us what evidence, level of reproducibility and reporting format they require so we can account for these during scoping.
How to get started
Tell us who the documentation is for and what it needs to explain. If helpful, include an existing dataset, a reporting format or a deadline. We can discuss the detailed requirements together.
Common questions
Can documentation support a regulatory submission?
Protocols, QC data and method reports can be prepared with an intended submission in mind. The specific requirements and suitability of the work must be agreed for each project. Tell us the intended use and applicable requirements when you contact us.
Can reporting be included in a laboratory project?
Yes. Clear documentation is part of our approach to experimental work. The project scope should specify the protocols, data, analyses and reports to be delivered.