E-drug: old drugs review procedures?
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Like many countries, South Africa registered all drugs on the market
when it started drug registration many years ago.
The European Union asked all member states to review
these 'old' drugs before 1994.
As the South African Drug Regulatory Authority will most probably
also embark on such a process, we would be interested to know from
other countries what their exact procedures and experiences were in
dealing with this backlog of 'old' drugs. Your feedback will be given
to MCC and DOH for their perusal.
kind regards
Wilbert Bannenberg
SADAP coordinator
Wilbert Bannenberg, SADAP Coordinator
Hallmark 938, P/Bag X 828, Pretoria 0001, South Africa
Tel work +27-12-3120374/5 Fax +27-12-3244525 Cellphone +27-82-5756249
Email 73377.3055@compuserve.com or bannew@hltrsa.pwv.gov.za
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