ZALIKA FARMACÊUTICA is a company
that is duly audited by ANVISA and has all licenses and authorizations
necessary to import, request registration (“Marketing Authorization”), store
and distribute pharmaceuticals, healthcare products and cosmetics. It also able
to request inspections of manufacturing plants abroad, as well as submit registration
dossiers to ANVISA.
ZALIKA FARMACÊUTICA has all infrastructure required by the Brazilian
legislation to hold registration of foreign companies, involving a portfolio of
products or even only one product, and covering a broad scope of healthcare
segments.
ZALIKA FARMACÊUTICA has built a Singular Platform for the entry strategy of
foreign companies into the Brazilian market, where the product registration
remains under total control of the foreign company, reducing timelines and
costs involved, which are usually significantly high.
ZALIKA FARMACÊUTICA technical complex has been planned and built assuming high
technological standards. ZALIKA has the Certificate of Good Storage and
Distribution Practices issued by ANVISA (CBPDA).
This technological complex comprises a quality control laboratory, a 12
thousand-square meter storage area, cold rooms, fleet for air and road
transportation, and a technical staff comprising qualified professionals that
are periodically trained to be able to perform their duties.
Besides all technical structure, which includes the Regulatory Affairs team
that is in charge of preaudit processes and adaptation of manufacturing plant
overseas to the Brazilian law, as well as preparation and submission of
technical dossiers, there is also the Medical Department, which conducts
metanalysis for innovative products and an efficient pharmacovigilance system
implemented.
ZALIKA FARMACÊUTICA! An option for a safe, agile, economical and
efficient entry into the Brazilian Healthcare Market.
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