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| Reporting guideline provided for? (i.e. exactly what the authors state in the paper) |
Reporting the chemical composition of medicinal plant extracts used in pharmacological, toxicological and clinical research studies. |
| Full bibliographic reference | Heinrich M, Jalil B, Abdel-Tawab M, Echeverria J, Kulić Ž, McGaw LJ, Pezzuto JM, Potterat O, Wang JB. Best Practice in the chemical characterisation of extracts used in pharmacological and toxicological research-The ConPhyMP-Guidelines. Front Pharmacol. 2022;13:953205. |
| Language | English |
| PubMed ID | 36176427 |
| Relevant URLs (full-text if available) |
Read the full-text of the ConPhyMP reporting guideline. |
| Reporting guideline acronym | ConPhyMP |
| Study design | Clinical trials, Experimental studies |
| Clinical area | Complementary and alternative medicine, Pharmaceutical medicine, Toxicology |
| Applies to the whole report or to individual sections of the report? | Harms/adverse effects/safety data, Intervention (exposure), Terminology/definitions |
| Additional information | An online fillable open-access ConPhyMP tool is also available via the GA (Society of Medicinal Plants and Natural Products Research) website at https://ga-online.org/best-practice/ |
| Record last updated on | August 16, 2023 |