Procurement
law set to lock in domestic bias for drug sales
A new
regulation on drug purchase priorities in the revised Law on Public
Procurement will help protect local drug producers.
The new law on public procurement seems to clearly favour domestic pharmaceutical producers Photo: Le Toan
Adopted by the National Assembly last November and to
take effect on July 1, the law stipulates that all locally-made drugs meeting
the Ministry of Health’s requirements on treatment, prices and supply can be
put out to tender and that equivalent imported drugs will not be allowed to
go to tender.
Last year
“Any bidding dossier that includes imported drugs will
be rejected. As we can now produce many types of drugs locally, we will not
allow the same products from foreign manufacturers,” said Ministry of
Planning and Investment’s Public Procurement Department head Le Van Tang.
Under Article 50, drug tenders will receive incentives
when they engage in local or international bidding to supply drugs of which
domestic production cost is at least 25 per cent of the products’ total cost.
Drug producers with at least 25 per cent female or 25
per cent wounded veterans or disabled people as a proportion of their
workforce would also be given priority, as well as small and medium-sized
enterprises.
“The government will describe these priorities in more
detail,” Tang said, adding “These regulations will have local drug producers
rejoicing, but will enrage drug importers.”
“We are happy with this regulation, as it helps protect
locally-produced pharmaceuticals, which have faced serious competition from
imported products,” said Le Van Truyen, former Deputy Minister of Health and
a representative for SAVI Pharmaceutical Joint Stock Company.
A representative from Lynh Pharma, which imports around
40 types of drugs into
“All active elements for drug making in
She said
According to her, in the coming months local
authorities will apply regulations on examining all imported drugs before
they receive customs clearance.
The new regulations are expected to be a big challenge
for importers, as it will take several months for the complete examination of
a single drug.
“These examinations are going to be a major burden on
importers,” the representative said.
Under
According to London-headquartered proprietary data,
analysis and ratings provider Business Monitor International,
By Thanh Dat, VIR
|
Thứ Hai, 14 tháng 4, 2014
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