E-drug: Legislation about Magistral Formulation
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Dear co-listers:
I'm writing from Argentina, from the Pharmaceutical Drug Information
Center of the College of Pharmacists of the Province of Buenos Aires.
I'm needing some information about the preparation of Magistral
Formulas in your countries. So, I've prepared some questions. I
would be very thankful to
receive your answers.
1) In which countries exist Official Vademecums containing Magistral Formulas?
2) How is drug quality control done? Which are the requirements the
drug providers must fulfill about the quality of the drugs they sell?
3) Is there Legislation concerning to Magistral Formulation?
(i.e.specifications about the place and minimal materials and
equipment in a laboratory, good manufacturing practices, etc.)
Daniel Eduardo Domosbian
Pharmaceutical Drug Information Center
College of Pharmacists of the Province of Buenos Aires
cimf@colfarma.org.ar
[These issues have been discussed on e-drug using different
terminology. It would be worth looking at the archives. Very
user-friendly searchable archives can be found at:
http://www.healthnet.org/programs/edrug.html BS]
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