Veyong Pasa iyo EU EDQM Audit Zvakare

Pana April 22, mashoko akanaka akasvika!Hebei Veyong Pharmaceutical Co., Ltd. zvakare vakabudirira kuwana EU CEP certificationivermectinAPI yakabudiswa neEuropean Agency yeHunhu hweMishonga (EDQM).

IvermectinAPI ndechimwe chezvigadzirwa zvikuru zveVeyong Pharma.Inogamuchirwa zvakanaka nevatengi kumba nekune dzimwe nyika nekuda kwekugadzikana kwayo kwakasimba, mhando yepamusoro uye kugadzirwa kwegirinhi.Muna 2018, yakabudirira kuwana iyo US FDA certification.

Chitupa che ivermectin CEP ndiyo European Pharmacopoeia adaptability certificate, iyo isingango zivikanwa nenyika dzese dziri nhengo dzeEU, asi inozivikanwawo nenyika dzakawanda dzinoziva chimiro cheEuropean Pharmacopoeia.Kuwana chitupa cheCEP zvakare kucherechedzwa kwezvigadzirwa zveVeyong Pharma mumusika wepasi rose, chimiro chemakwikwi emusika weVeyong, uye chiratidzo chakakosha chekuwana budiriro yebhizimusi repamusoro mumisika yemhiri kwemakungwa.