You cannot use someone else’s for this, you need to design it yourself. The design is based on quality standards or SOPs.

It is better to design a fill-in-the-blank type. Taking HPLC as an example, it should include the following elements:

1. Chromatographic conditions: chromatographic column type, mobile phase composition and ratio, detection Wavelength, injection volume, system suitability requirements (number of theoretical plates, resolution, etc.), some also include column temperature, flow rate, etc. If it is not a UV detector, the conditions of the detector must also be noted;

2. Preparation of reference substance: weighing sample amount, processing method (such as reduced pressure drying time, temperature, etc.), purity, dilution and volume steps

3. Preparation of test sample: weighing Sample volume, pretreatment, dilution and volume steps

4. Calculation formula

5. Qualification standards

6. Result judgment

7. Signature (tester, reviewer)

Leave spaces for the parameters, data, and signatures that need to be recorded, and just fill them in during use. The chromatogram is attached to the back of the record.

It should be very detailed. I believe you can make it quickly.