Enablement in Invention Disclosures: What to Include
Not legal advice. Align with your counsel’s standards.
What is Enablement (in practice)
- Provide enough detail so a person skilled in the art can make and use the invention without undue experimentation.
- Focus on concrete parameters, steps, materials, and conditions—not only concepts.
Data and Parameters
- Define ranges and tolerances: “buffer pH 7.2–7.6,” “window size 20–50ms,” “torque 0.7–1.1Nm.”
- Environmental conditions: temperature, humidity, EMI, vibration, latency budgets.
- Dependencies and versions: libraries, firmware, assay kits, calibration procedures.
Reproducibility Tips
- Provide at least one fully specified embodiment with acceptance criteria.
- Include negative results and boundary conditions that motivated design choices.
- Describe controls, benchmarks, and how data was collected/processed.
Domain Pointers
- Software: data schemas, time/space complexity, concurrency model, cache/consistency, security controls.
- Medical devices: materials, biocompatibility notes, power limits, sampling rates, filter settings, calibration.
- Biotech: strain/cell line, reagent sources, timings, temperatures, controls, analysis methods.
- Mechanical/Robotics: tolerances, duty cycles, kinematics, PID gains, environmental ratings.
Common Gaps to Avoid
- Vague adjectives without numbers (“fast,” “robust”).
- Missing environment/setup information and unversioned dependencies.
- No acceptance criteria or test method.
Mini Checklist
- One complete embodiment
- Parameter ranges and units
- Figures referenced in text
- Data or rationale for key choices
- Attachment list with versions