검색어: scientific (영어 - 텔루구어)

scientific
శైన్విక

scientific name
శాస్త్రీయ పేరు

ragi scientific name
రాగి శాస్త్రీయ నామం

chikkudu scientific name
చిక్కడు శాస్త్రీయ పేరు

scientific name of plants
మొక్కల శాస్త్రీయ పేరు

chikkudu scientific name english
చిక్కుడు శాస్త్రీయ నామం ఆంగ్లం dolichus lablab

scientific name of banthi flower
బంది పువ్వు యొక్క శాస్త్రీయ నామం

scientific name of plants and animals
మొక్కలు మరియు జంతువుల శాస్త్రీయ పేరు

pyabesi plants scientific name in telugu
తెలుగులో పైబేసి మొక్కల శాస్త్రీయ నామం

kandhi scientific name of plants and animals
kandhi

scientific name of plants and animals beech
మొక్కలు మరియు జంతువులు శాస్త్రీయ పేరు

scientific name of gunugu puvvu flower in telugu
తెలుగులో తునుగు గులాబి పువ్వు యొక్క శాస్త్రీయ పేరు

research in simple terms,refers to a search for knowledge.it is also known as a scientific and systematic search for information on particular topic or issue.
సాధారణ పరంగా పరిశోధన, విజ్ఞానం కోసం ఒక శోధన సూచిస్తుంది

article 58 of the regulation responds to the need to protect public health and to give scientificassistance to non-member countries in the context of cooperation with who whilst at the same timeallowing rapid access to those countries for important new medicinal products.
రెగ్యులేషన్ ఆర్టికల్ 58 ప్రజారోగ్య రక్షించడానికి మరియు సహకారంతో సందర్భంలో సభ్యులు కాని దేశాలలో శాస్త్రీయ అందజేయటం అవసరం స్పందిస్తుంది who ముఖ్యమైన కొత్త ఔషధ ఉత్పత్తులను కోసం ఆ దేశాలకు వేగవంతమైన ప్రాప్తిని అనుమతిస్తూ అదే సమయంలో.

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