Guest guest Posted July 19, 2005 Report Share Posted July 19, 2005 Dear Friends in GIPA Alliance & Forum It is encouraging to see at that at least the civilv society is invited to a meeting. What is not surprising is that according to the posting, I quote, " The ARV drugs that is in receipt seems to be of triple combination viz. Stavudine, lamivudine nevirapine and zidovudine, lamivudine, Nevirapine along with some 50 slots for effavirenz. " Now my concern is the transparency of the functioning of the ART centre at RIMS. I remember we were facing irregularity in the supply of medication for the existing 200 or so who are on the list. Here are few questions that we need to address before scaling up the whole thing. 1. What steps are in place to ensure that supply of medicines to the beneficiaries are consistent? 2. Who would be responsible if these steps are not followed. 3. If the bottlenecks on the present disbursement systems are not addressed, would it not create more harm to individuals who would be enrolled afresh in the ARV disbursement programme. (Harm: in terms of in adequate supply of Medication, improper supply chain management, support systems) 4. Does the existing program need evaluation before expansion? can an independent body do it? How can this be made possible? 5. Not only the criterion of the beneficiaries, but the capability of the roll out centre should also be measured. 6. Proper supply chain management strategy should also be made before the expansion of the program. 7. Component of Dietary and Nutritional support and guidance should also be provided along side with the expansion. I hope the concerns raised here in the previous posting and few added on here are addressed before we make any expansion. In solidarity, E-mail: jon.lall@... Quote Link to comment Share on other sites More sharing options...
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