Vous avez cherché: i am at least 18 years old (Anglais - Télougou)

are you at least 18 years old?
మీరు 18 సంవత్సరాల కంటే ఎక్కువ వయస్సు ఉన్నారా

i am 17 years old
నా వయస్సు 17 సంవత్సరాలు

are you over 18 years old
నేను 18 సంవత్సరాల కంటే పెద్దవాడిని

i am older than 18 year old
నేను 18 సంవత్సరాల కంటే పెద్దవాడిని

i am at home
మీ langage పూర్తి వాక్యం టైప్

i am 7 year old
నేను ఒక అమ్మాయిని

i am at the hyderabad
నేను బెంగుళూరులో ఉన్నాను

i am at 4th floor sir
nenu 4th floor unanu sir

i am at work, give me some ��������
కొంత సమయం ఇవ్వండి

i am at home i will call u tomorrow
మీరు తప్పిపోయారు

thank you god i am completed my 17 years i am started my 18 years only your grace
దేవుడికి ధన్యవాదాలు నేను 17 సంవత్సరాలు పూర్తి చేసుకున్నాను నేను 18 సంవత్సరాలు ప్రారంభించాను మీ కృప మాత్రమే

consent form - i participants information sheet (pis) information for participants of the study. instructions - this is the patient information sheet. it should address the participant of this study. depending upon the nature of the individual project, the details provided to the participant may vary. a separate consent form for the patient/test group and control (drug/procedure or placebo) should be provided as applicable. while formulating this sheet, the investigator must provide the following information as applicable in a simple language in english and telugu which can be understood by the participant • title of the project ___________ • name of the investigator/guide _________ • purpose of this project/study ____________ • procedure/methods of the study _____________ • expected duration of the subject participation ______________ • the benefits to be expected from the research to the participant or to others and the post trial responsibilities of the investigator ______________ • any risks expected from the study to the participant _____________ • maintenance of confidentiality of records ______________ • provision of free treatment for research related injury ___________ • compensation of the participants for disability or death resulting from such injury __ • freedom to withdraw from the study at any time during the study period without the loss of benefits that the participant would otherwise be entitled __________ • possible current and future uses of the biological material and of the data to be generated from the research and if the material is likely to be used for secondary purposes or would be shared with others, this should be mentioned ________ • address and telephone number of the investigator and co-investigator/guide ________ • the patient information sheet must be duly signed by the investigator ___________ --------x---------- consent form - ii participant informed consent form (picf) participant’s name: address: title of the project: the details of the study have been provided to me in writing and explained to me in my own language. i confirm that i have understood the above study and had the opportunity to ask questions. i understand that my participation in the study is voluntary and that i am free to withdraw at any time, without giving any reason, without the medical care that will normally be provided by the hospital being affected. i agree not to restrict the use of any data or results that arise from this study provided such a use is only for scientific purpose(s). i have been given an information sheet giving details of the study. i fully consent to participate in the above study. signature of the participant: ______________________ date: _____________ signature of the witness: ________________________ date: _____________ (note: consent form ii should be appropriately worded for adults and children (less than 18 years) e.g. if the participant is less than 18 years of age, instead of ‘my participation’, ‘my child’s/ward’s participation’ needs to be replaced.)
ఔషధాన్ని రూపం