نتایج جستجو برای: medicinal application
تعداد نتایج: 800237 فیلتر نتایج به سال:
Epilepsy is a condition in which a person has recurrent seizures. The mainstay of treatment for epilepsy remains symptomatic despite the rapid expansion in knowledge of its neurological disabilities. Therapeutic options, both medical , surgical and non medical have been markedly improved over the past decades, resulting in better condition, activities of daily living, and quality of life for ep...
for centuries, herbal drugs have been the only accessible resource for treatment of pain and passions. today, despite remarkable progress and development of synthetic drugs, medicinal plants and their derived drugs are used massively. so that, in some countries medicinal plants is inseparable from drugs and treatment systems. more ever, their marketing and economical aspects are more flourishin...
A survey of medicinal plants used by rural and urban inhabitants of the three cities of the Tropical Atlantic Forest, Region of Vale do Ribeira, State of São Paulo, Brazil was performed by means of 200 interviews with medicinal plant users and extractors and, traditional healers. One hundred fourteen herbal remedies were recorded and the following information reported: Latin, vernacular and Eng...
Hortus Malabaricus is the oldest important printed book on Indian medicinal plants. The 1(st) of its 12 volumes was published in 1678 from Amsterdam this book, written by H.A. Van Rheede is perhaps the only authentic record of the ethnoiatrical knowledge of ancient Malabar, available to us today. Several hundred medicinal plants which were successful used by the Ayurvedic physiclans of 17(th) c...
Guideline Title Non-clinical Local Tolerance Testing of Medicinal Products Legislative basis Directive 75/318/EEC as amended Date of first adoption December 1990 Date of entry into force June 1991 Status Last revised 1990 Previous titles/other references Local Tolerance Testing of Medicinal Products III/3979/88 Additional Notes This note for guidance concerns the application of part 3, section ...
BACKGROUND In order to facilitate multinational clinical research, regulatory requirements need to become international and harmonised. The EU introduced the Directive 2001/20/EC in 2004, regulating investigational medicinal products in Europe. METHODS We conducted a survey in order to identify the national regulatory requirements for major categories of clinical research in ten European Clin...
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