UNICENTA is made of placenta with its safety strictly and perfectly secured in all its production processes.
Production Process
Pharmaceutical companies that are approved for compliance with regulations on production and quality control of placenta based medicine by the Ministry of Food and Drug Safety can produce it.
However, in accordance with the Article 31 of the Pharmaceutical Affairs Act, human placenta medicine should be produced or manufactured by BGMP certified companies as ingredients for medicine only.
We collect placenta from healthy pregnant women who had agreed to collection and medical examination to donate their placenta.
We select medical institutions with excellent capacity to supply placenta based on our investigation.
We collect placenta with its safety secured only through strict safety check system (virus examination).
We produce human placenta based medicine products through a series of safety tests including virus examinations, sterilization and hydrolysis covering from processing of raw ingredients (placenta) to production of finished ones.
It’s because we perform examination and inactivation of viruses in every process and provide medicine with its safety verified through sterilization test.
The Ministry of Food and Drug Safety implements “DMF (Drug Master File)” to control quality and safety of human placenta based medicine products covering from production to packaging and (distribution) management.
UNICENTA is a medicine with its safety and validity verified by the Ministry of Food and Drug Safety through clinical tests in Korea.
UNIMED PHARM Inc. has been involved in production of OTC and ETC medicines for the past 30 years and started to produce UNICENTA sol. and inj. based on DMF certification by the Ministry of Food and Drug Safety and strict criteria of clinical retest while providing placenta ingredients and finished ones to renowned pharmaceutical companies in Korea.
UNICENTA is human placenta based OTC/ETC medicine safely produced from raw ingredient processing to production under supervision of the Ministry of Food and Drug Safety.
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