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RES INSTITUTE OF PRC NATIONAL HEALTH AND FAMILY PLANNING COMMISSION

Overview
  • Total Patents
    31
  • GoodIP Patent Rank
    51,472
  • Filing trend
    ⇧ 88.0%
About

RES INSTITUTE OF PRC NATIONAL HEALTH AND FAMILY PLANNING COMMISSION has a total of 31 patent applications. It increased the IP activity by 88.0%. Its first patent ever was published in 2016. It filed its patents most often in China. Its main competitors in its focus markets biotechnology, organic fine chemistry and pharmaceuticals are QINGDAO SITUO XINYUAN CELL MEDICINE CO LTD, BGI SHENZHEN and THE GOVERNMENT OF THE US SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES CENTERS FOR DISEAS.

Patent filings in countries

World map showing RES INSTITUTE OF PRC NATIONAL HEALTH AND FAMILY PLANNING COMMISSIONs patent filings in countries
# Country Total Patents
#1 China 31

Patent filings per year

Chart showing RES INSTITUTE OF PRC NATIONAL HEALTH AND FAMILY PLANNING COMMISSIONs patent filings per year from 1900 to 2020

Top inventors

# Name Total Patents
#1 Ma Xu 17
#2 Gao Huafang 8
#3 Cao Zongfu 7
#4 Li Peng 6
#5 Ning Lifeng 6
#6 Jin Xiaohua 5
#7 Qiu Shunchen 5
#8 Lu Jianbo 5
#9 Chen Xiaofeng 4
#10 Wang Huiping 4

Latest patents

Publication Filing date Title
CN109762846A GALC relevant to Krabbe disease is repaired using base editorC1586TThe reagent and method of mutation
CN109706185A The method and application of gene knockout are realized based on base editing system mutation initiation codon
CN109666673A It is repaired using base editor and stores up the relevant E8SJM of disease to cholesteryl ester-1G>AThe reagent and method of mutation
CN109777832A MAN2B1 relevant to mannosidosis is repaired in base editor simulationC2248TThe reagent and method of mutation
CN109628567A It is a kind of for detecting the non-invasive antenatal detection system of fetal chromosomal aneuploidy
CN109300501A Prediction method for three-dimensional structure of protein and the prediction cloud platform constructed with it
CN109086574A Disease related protein database
CN109086571A A kind of method and system that monogenic disease hereditary variation is intelligently interpreted and reported
CN109306376A Examine the quality control standard product and preparation method thereof of nucleic acid amplification homogeneity
CN109119132A Method and system based on case history characteristic matching monogenic disease title
CN110664730A Slow-release microneedle patch with large drug-loading rate and containing insoluble contraceptive and preparation method thereof
CN109002833A A kind of microlayer model data analysing method and system
CN108531580A C5orf42 gene mutation bodies and its application
CN108794555A A kind of ethinyloestradiol pharmaceutical co-crystals and preparation method thereof
CN108623648A Nomegestrol acetate crystal form I and its preparation method and application
CN108467420A A kind of Nomegestrol acetate crystal form II and preparation method thereof
CN108342404A INPP5E gene mutation bodies and its application
CN108090326A The construction method of unicellular network regulation relation
CN108085384A Heredity angiocardiopathy detection method
CN108334751A A kind of method and device of substance for calculation concentration