Original research should be designed in accordance with the IMRAD format.

The editorial board strongly recommends observing the following standards for the presentation of their scientific research, depending on its type:

• parallel group randomized trials – CONSORT standard;

• observational studies – STROBE standard;

• clinical trials – SPIRIT standard;

• diagnostic accuracy studies – STARD standard;

• clinical case reporting – CARE standard;

• clinical practice guidelines – AGREE standard;

• qualitative research – SRQR standard;

• preclinical animal studies – ARRIVE standard;

• quality improvement reporting SQUIRE standard;

• health economic evaluation reporting – CHEERS

All clinical and preclinical studies must be approved by the ethics committee.

All studies involving vulnerable populations should be conducted in accordance with international ethical principles.

The conclusion of the ethics committee is obligatory if any biomaterials were collected.

The editorial board has the right to request from the authors a copy of the conclusion of the ethics committee. Researchers must obtain voluntary informed consent from patients or their legal representatives to participate in the study.

Consent form-must be approved by the ethics committee.

Full information is presented in the Ethical Code of the "Eco-Vector" publishing house.