HerbResearch covers a large spectrum of activities in cooperation with France-based Medicinal & Aromatic Plants R&D. This spectrum reaches from quality assurancep rojects and pharmacological, toxicological, and clinical questions to support in regulatory affairs. We have access to the most important medicinal databases and to a well-organised network of external consultants for specific projects (e.g. certifications). Herbresearch and Medicinal & Aromatic Plants R&D also work on own research projects with various herbs.
Herbal Medicine Clinical Research
Another focus of our work is on medical writing. We contribute to all stages of:
Clinical research:
- Creation of study reports of clinical trials and observational studies
- Evaluation of study reports and statistical reports for the creation of original publications
- Creation of publication manuscripts (English/German/French)
- Evaluation of new studies on (in-)efficacy and adverse effects of herbal medicines, and scientific-journalistic support
Drug registration support
- We can provide phytotherapeutic information in support of the choice of ingredients in a given product.
- Creation of registration dossiers in CTD format for the segments of quality, pharmacology and clinical application.
Our spectrum of scientific service includes
Literature research
- Translations of scientific contributions (French/Spanish/Italian)
- Poster presentations at international conferences
- Oral presentations in English/German/French/Spanish
- Marketing support
- Easily understandable scientific arguments in legal matters
Pharmacology/Toxicology review
HerbResearch is involved in the organisation of a number of toxicological and pharmacological studies, beginning with the planning and mediation down to the evaluation and publication. We also offer literature research and expertises in toxicological and pharmacological evaluations of herbal preparations. We also work on the differentiation of pharmacological versus physiological effects of food supplements, and on the toxicity of herbal raw material.
Pharmacovigilance
An important part of our work in relation to pharmacovigilance is the creation of Periodic Safety Update Reports (PSUR) in drug registration, including literature research and the procurement of the original papers.
We have ample experience in the evaluation of case reports of adverse effects (AE). For a number of medicinal plants we already created detailed analyses of case data of adverse effects related to drug safety protocols.
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