Therapeutic and pharmaceutical aspects of so-called non-regular medical treatment (anthroposophy, homoeopathy, phytotherapy etc.) were investigated by means of an inquiry directed to the suppliers of non-regular drugs. Data of 17 respondents are condensed into two tables and discussed in the light of the Medicines Supply Act. It is concluded that the pharmacist has to inform himself carefully about the non-regular preparations before he decides to supply them to the patient. It is concluded that the Drug Authorities should enforce five requirements regarding these preparations.
SAMENVATTINGEen onderzoek werd ingesteld naar therapeutische en farmaceutische aspecten van niet-reguliere behandelingsmiddelen en hun leveranciers. De gegevens van zeventien leverancicrs werden samengevat in tabel II en nt en besproken, mede in het licht van de Wet op de Geneesmiddelenvoorziening. Geconcludeerd wordt dat de apotheker, wil hij genoemde middelen afleveren, zich zorgvuldig moet informeren bij de leverancier. In vijf punten worden eisen, die de Overheid aan dit soort middelen zou moeten stellen, samengevat.
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