I-Ritamedtech (Zhongshan) Limited (ngemuva kwalokhu ebizwa ngokuthi i-Ritamedtech) yasungulwa ngo-2023. Iyingxenye ye-Hongrita Group esebenza ngokukhethekile embonini yezokwelapha, ehlinzeka ngezixazululo ezibanzi zokukhiqiza zokubumba ze-Class I kuya ku-Class III yedivayisi yezokwelapha kanye nezingxenye ezinembayo namamojula amaklayenti adumile emhlabeni jikelele.

I-Ritamedtech isebenzisa i-Class 100,000 (ISO 8) GMP Cleanroom eqinisekisiwe kanye ne-Class 10,000 (ISO 7) GMP Laboratory, uhlelo lwe-air-conditioning oluhlanzekile lwe-HEPA oluhlonyiswe nge-HEPA, uhlelo lokuhlanza amanzi, uhlelo lokuqapha imvelo, kanye nezindawo zokuvala inzalo ezindaweni zokukhiqiza. Inkampani igcina amandla angaphakathi endlini okuhlola ubunyumba, ukuqinisekiswa kwe-bioburden, nokuhlaziywa kwezingxenye, okusekelwa Uhlelo Lokuphathwa Kwekhwalithi Ye-ISO13485 oluqinisekisiwe. Lolu hlaka oludidiyelwe luqinisekisa ukuthobelana okugcwele Nomkhuba Wokukhiqiza Okuhle Kwedivayisi Yezokwelapha yaseChina (MDGMP 2014), Imfuneko Yokuphatha Ye-Aseptic Medical Device Manufacturing (YY 0033-2000), Ikhodi Yokuklanywa Kwamagumbi Okuhlanza (GB 50073-2013), Ikhodi Yokwakhiwa Kwamakamelo Ahlanzekile05 kanye Nokwamukelwa10 kwe-US1-1GB I-FDA 21 CFR Ingxenye 820—Ukulawulwa Kwesistimu Yekhwalithi.