• RESEARCH 4 BUSINESS 2016, Ljubljana, 5 and 6 of May 2016

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    CONCLUSION Botanical sildenafil generic release date products are used worldwide. The production of good quality dietary supplements is of 12 An Introduction to Botanical Medicines utmost importance in order for clinical trials to establish the safety and efficacy of these supplements. Numerous initial clinical trials are being attempted worldwide to ascertain these safety and efficacy issues, as we will see later in this book.

    The FDA routinely evaluates these preparations, and where safety concerns are present (such as the case with ephedra), the FDA has the duty and responsibility to ban the products from the market. Until the botanical products undergo rigorous clinical testing employing the gold standard in clinical research, randomized placebocontrolled clinical trials, safety and efficacy issues will remain unanswered. Perhaps the best monitoring device is one that is created by the dietary supplements industry itself to police itself and establish “standards for practice.” Therefore, “bad apples” may be eliminated from their midst.

    Botanicals should be considered “diluted” forms of drugs and should thus be respected with regard to their effects on various human body systems. In the United States, the official status of botanicals is that of dietary supplements. Other responsible organizations, such as the U.S.P., are working on improving the quality of these products.

  • Natural and artificial systems sildenafil generic release date. O., Burgess, R. (1975). H. Ikeda, A., Lüders, H.

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    23. Mofidi R, Duff MD, Wigmore SJ, et al.