Medical Laser, the ASAlaser partner for Australia, is always at the forefront in spreading our healthcare solutions thanks to an active and expert team which continues to reap positive feedback from the many events it participates in.
In Hindmarsh (South Australia), from 2nd to 4th June, it took part in the Australian Podiatry Association conference entitled "Pain Free", held in the Adelaide Entertainment Centre premises, which was attended by around 200 delegates from South Australia. For the occasion, in addition to the exhibition area in which it promoted the ASAlaser devices, the Medical Laser staff organised a workshop to show the results of the scientific research at the base of the MLS® Laser Therapy. This was followed by an interesting practical session on real patients.
In late July, Medical Laser attended another fruitful event: the 8th edition of the annual Symposium organized by AAFN (Australasian Academy of Functional Neurology) at the Kiribilli Club in Lavender Bay in Sydney. A three-day event, from 29th to 31st July, entitled "Bridging the gaps with Brain-Based Therapies" which our dealer attended as sponsor. In addition, for the occasion, podiatrist Bronwyn Cooper, founder of the "Dr Foot Solutions" chain of clinics and Dr Scott Wustenberg, BSc. Chiro, BSc. Physiol, MSc Nut Med, both users of MLS® Laser Therapy, were present at the stand in order to testify to the validity of our therapy in clinical practice.
"During these two recent events, there was a great deal of interest shown towards our equipment -said Michelle Davis, the Managing Director of Medical Laser- Constant exposure of MLS® Laser Therapy and positive outcomes encourage us to continue along this line of dissemination".
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Decreto Legislativo 24 febbraio 1997, n°46 Articolo 21
1. E' vietata la pubblicità verso il pubblico dei dispositivi che, secondo disposizioni adottate con decreto del Ministro della Sanità, possono essere venduti soltanto su prescrizione medica o essere impiegati eventualmente con l'assistenza di un medico o di altro professionista sanitario.
2. La pubblicità presso il pubblico dei dispositivi diversi da quelli di cui al comma 1 è soggetta ad autorizzazione del Ministero della Sanità. Sulle domande di autorizzazione esprime parere la Commissione di esperti prevista dall'articolo 6, comma 3, del decreto legislativo
30 dicembre 1992, n. 541, che a tal fine è integrata da un rappresentante del Dipartimento del Ministero della Sanità competente in materia di dispositivi medici e da uno del Ministero dell'Industria, del commercio e dell'artigianato.
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