Guest guest Posted January 3, 2012 Report Share Posted January 3, 2012 WHICH BONE GROW BY ENDOCHONDRAL OSSIFICATION ONLY ? From: Zahid Ahmad <zahiddentalsurgeon@...> Sent: Friday, 30 December 2011, 21:18 Subject: RE: Consent Explicit Consent is taken for survey ,study or resarch purpose for the use of collected data only:To use personal data lawfully you must comply with all UK laws, and meet one condition from the list of conditions set out in the data Protection Act. To use sensitive personal data you must also meet one condition from the additional list of conditions. The conditions that are most likely to apply for research using any personal data are:You have obtained consent from the data subject.You are processing personal data for the legitimate interests of the Organisation or a third party and your use does not cause unwarranted prejudice to the rights and freedoms, or the legitimate interests of the data subject.The conditions that are most likely to apply for research using sensitive personal data are:You have obtained “explicit consent†from the data subject. Explicit consent must be freely given, specific and informed; see below for guidance on obtaining explicit consent.You are carrying out medical research and you are a health professional or someone who owes a similar duty of confidentiality (for example a scientist employed by a health service body). If you choose this condition you will also need to take into account medical ethics and confidentiality constrainYou are analysing racial /ethnic origins for equal opportunities purposes.Your processing of sensitive personal data “is in the substantial public interest and is necessary for research purposes and does not support measures with respect to the particular data subject except with their specific consent nor cause or be likely to cause substantial damage and distress†(The Data Protection (Processing of Sensitive Personal Data) Order 2000). For example, the transmission of relevant patient files by hospitals to local authority cancer registries is in the substantial public interest, because it is vital in protecting and enhancing the public health. If you think that your research may be in the substantial public interest you should include a statement in your initiation document (or equivalent) indicating the potential benefits to the public of your research. However, the substantial public interest is a very high test so you should only use this condition with caution.In most cases where you are using sensitive personal data you will use the explicit consent condition. For consent to be explicit individuals must have a full understanding of what you intend to do with their data and they must “opt-inâ€; you cannot ask them to opt-out if they object. You should keep a record that you have received explicit consent from the individual whose data you are using. The method you chose to use to collect explicit consent will depend upon the nature of your research but you may choose to:Ask individuals to sign a consent form..If you are asking individuals to complete a questionnaire you may decide to include a data protection statement within the questionnaire and ask individuals to sign to say they consent.Hope it helpDr.Zahid From: huraira2002@...Date: Fri, 30 Dec 2011 16:58:21 +0000Subject: Consent I can't find explicit consent anywhere can someone shed som light pls? What is it? And when do we need it(what situations)Sent from my BlackBerry wireless device from MTNFrom: "drbaghyarani" <drbaghyarani@...> Sender: Date: Fri, 30 Dec 2011 14:23:27 -0000< >Reply Subject: Regarding and Hi friends I ve recently started from Anatomy. What are all the chapters do we need in and ? Shall i go through the developmental anatomy in this book or any other book? Any questions from thorax? Please guide me... any help will be much appreciated. Thanks and regards Rani Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2012 Report Share Posted January 3, 2012 its TEMPORAL bones. From: ARTHUR TADEVOSYAN <arthur_tadevosyan@...> " " < > Sent: Tuesday, 3 January 2012 7:57 PM Subject: Re: Consent WHICH BONE GROW BY ENDOCHONDRAL OSSIFICATION ONLY ? From: Zahid Ahmad <zahiddentalsurgeon@...> Sent: Friday, 30 December 2011, 21:18 Subject: RE: Consent Explicit Consent is taken for survey ,study or resarch purpose for the use of collected data only:To use personal data lawfully you must comply with all UK laws, and meet one condition from the list of conditions set out in the data Protection Act. To use sensitive personal data you must also meet one condition from the additional list of conditions. The conditions that are most likely to apply for research using any personal data are:You have obtained consent from the data subject.You are processing personal data for the legitimate interests of the Organisation or a third party and your use does not cause unwarranted prejudice to the rights and freedoms, or the legitimate interests of the data subject.The conditions that are most likely to apply for research using sensitive personal data are:You have obtained “explicit consent†from the data subject. Explicit consent must be freely given, specific and informed; see below for guidance on obtaining explicit consent.You are carrying out medical research and you are a health professional or someone who owes a similar duty of confidentiality (for example a scientist employed by a health service body). If you choose this condition you will also need to take into account medical ethics and confidentiality constrainYou are analysing racial /ethnic origins for equal opportunities purposes.Your processing of sensitive personal data “is in the substantial public interest and is necessary for research purposes and does not support measures with respect to the particular data subject except with their specific consent nor cause or be likely to cause substantial damage and distress†(The Data Protection (Processing of Sensitive Personal Data) Order 2000). For example, the transmission of relevant patient files by hospitals to local authority cancer registries is in the substantial public interest, because it is vital in protecting and enhancing the public health. If you think that your research may be in the substantial public interest you should include a statement in your initiation document (or equivalent) indicating the potential benefits to the public of your research. However, the substantial public interest is a very high test so you should only use this condition with caution.In most cases where you are using sensitive personal data you will use the explicit consent condition. For consent to be explicit individuals must have a full understanding of what you intend to do with their data and they must “opt-inâ€; you cannot ask them to opt-out if they object. You should keep a record that you have received explicit consent from the individual whose data you are using. The method you chose to use to collect explicit consent will depend upon the nature of your research but you may choose to:Ask individuals to sign a consent form..If you are asking individuals to complete a questionnaire you may decide to include a data protection statement within the questionnaire and ask individuals to sign to say they consent.Hope it helpDr.Zahid From: huraira2002@...Date: Fri, 30 Dec 2011 16:58:21 +0000Subject: Consent I can't find explicit consent anywhere can someone shed som light pls? What is it? And when do we need it(what situations)Sent from my BlackBerry wireless device from MTNFrom: "drbaghyarani" <drbaghyarani@...> Sender: Date: Fri, 30 Dec 2011 14:23:27 -0000< >Reply Subject: Regarding and Hi friends I ve recently started from Anatomy. What are all the chapters do we need in and ? Shall i go through the developmental anatomy in this book or any other book? Any questions from thorax? Please guide me... any help will be much appreciated. Thanks and regards Rani Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2012 Report Share Posted January 3, 2012 Parotid gland development in utero in which month? Is it 7-8 months or 6 months?Sent from my BlackBerry® wireless deviceFrom: Kanika Kohli <kanika_sahil@...>Sender: Date: Wed, 4 Jan 2012 01:42:09 +0530 (IST) < >Reply Subject: Re: Consent its TEMPORAL bones. From: ARTHUR TADEVOSYAN <arthur_tadevosyan@...> " " < > Sent: Tuesday, 3 January 2012 7:57 PM Subject: Re: Consent WHICH BONE GROW BY ENDOCHONDRAL OSSIFICATION ONLY ? From: Zahid Ahmad <zahiddentalsurgeon@...> Sent: Friday, 30 December 2011, 21:18 Subject: RE: Consent Explicit Consent is taken for survey ,study or resarch purpose for the use of collected data only:To use personal data lawfully you must comply with all UK laws, and meet one condition from the list of conditions set out in the data Protection Act. To use sensitive personal data you must also meet one condition from the additional list of conditions. The conditions that are most likely to apply for research using any personal data are:You have obtained consent from the data subject.You areprocessing personal data for the legitimate interests of the Organisation or a third party and your use does not cause unwarranted prejudice to the rights and freedoms, or the legitimate interests of the data subject.The conditions that are most likely to apply for research using sensitive personal data are:You have obtained “explicit consent†from the data subject. Explicit consent must be freely given, specific and informed; see below for guidance on obtaining explicit consent.You are carrying out medical research and you are a health professional or someone who owes a similar duty of confidentiality (for example a scientist employed by a health service body). If you choose this condition you will also need to take into account medical ethics and confidentiality constrainYou are analysing racial /ethnic origins for equal opportunities purposes.Your processing of sensitive personal data “is in the substantial public interest and is necessary for research purposes and does not support measures with respect to the particular data subject except with their specific consent nor cause or be likely to cause substantial damage and distress†(The Data Protection (Processing of Sensitive Personal Data) Order 2000). For example, the transmission of relevant patient files by hospitalsto local authority cancer registries is in the substantial public interest, because it is vital in protecting and enhancing the public health. If you think that your research may be in the substantial public interest you should include a statement in your initiation document (or equivalent) indicating the potential benefits to the public of your research. However, the substantial public interest is a very high test so you should only use this condition with caution.In most cases where you are usingsensitive personal data you will use the explicit consent condition. For consent to be explicit individuals must have a full understanding of what you intend to do with their data and they must “opt-inâ€; you cannot ask them to opt-out if they object. You should keep a record that you have received explicit consent from the individual whose data you are using. The method you chose to use to collect explicit consent will depend upon the nature of your research but you may choose to:Ask individuals to sign a consent form..If you are asking individuals to complete a questionnaire you may decide to include a data protection statement within the questionnaire and ask individuals to sign to say theyconsent.Hope it helpDr.Zahid From: huraira2002@...Date: Fri, 30 Dec 2011 16:58:21 +0000Subject: Consent I can't find explicit consent anywhere can someone shed som light pls? What is it? And when do we need it(what situations)Sent from my BlackBerry wireless device from MTNFrom: "drbaghyarani" <drbaghyarani@...>Sender: Date: Fri, 30 Dec 2011 14:23:27 -0000< >Reply Subject: Regarding and Hi friendsI ve recently started from Anatomy.What are all the chapters do we need in and ? Shall i go through the developmental anatomy in this book or any other book?Any questions from thorax?Please guide me... any help will be much appreciated.Thanks and regardsRani Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2012 Report Share Posted January 8, 2012 THANK YOU From: Kanika Kohli <kanika_sahil@...> " " < > Sent: Tuesday, 3 January 2012, 20:12 Subject: Re: Consent its TEMPORAL bones. From: ARTHUR TADEVOSYAN <arthur_tadevosyan@...> " " < > Sent: Tuesday, 3 January 2012 7:57 PM Subject: Re: Consent WHICH BONE GROW BY ENDOCHONDRAL OSSIFICATION ONLY ? From: Zahid Ahmad <zahiddentalsurgeon@...> Sent: Friday, 30 December 2011, 21:18 Subject: RE: Consent Explicit Consent is taken for survey ,study or resarch purpose for the use of collected data only:To use personal data lawfully you must comply with all UK laws, and meet one condition from the list of conditions set out in the data Protection Act. To use sensitive personal data you must also meet one condition from the additional list of conditions. The conditions that are most likely to apply for research using any personal data are:You have obtained consent from the data subject.You are processing personal data for the legitimate interests of the Organisation or a third party and your use does not cause unwarranted prejudice to the rights and freedoms, or the legitimate interests of the data subject.The conditions that are most likely to apply for research using sensitive personal data are:You have obtained “explicit consent†from the data subject. Explicit consent must be freely given, specific and informed; see below for guidance on obtaining explicit consent.You are carrying out medical research and you are a health professional or someone who owes a similar duty of confidentiality (for example a scientist employed by a health service body). If you choose this condition you will also need to take into account medical ethics and confidentiality constrainYou are analysing racial /ethnic origins for equal opportunities purposes.Your processing of sensitive personal data “is in the substantial public interest and is necessary for research purposes and does not support measures with respect to the particular data subject except with their specific consent nor cause or be likely to cause substantial damage and distress†(The Data Protection (Processing of Sensitive Personal Data) Order 2000). For example, the transmission of relevant patient files by hospitals to local authority cancer registries is in the substantial public interest, because it is vital in protecting and enhancing the public health. If you think that your research may be in the substantial public interest you should include a statement in your initiation document (or equivalent) indicating the potential benefits to the public of your research. However, the substantial public interest is a very high test so you should only use this condition with caution.In most cases where you are using sensitive personal data you will use the explicit consent condition. For consent to be explicit individuals must have a full understanding of what you intend to do with their data and they must “opt-inâ€; you cannot ask them to opt-out if they object. You should keep a record that you have received explicit consent from the individual whose data you are using. The method you chose to use to collect explicit consent will depend upon the nature of your research but you may choose to:Ask individuals to sign a consent form..If you are asking individuals to complete a questionnaire you may decide to include a data protection statement within the questionnaire and ask individuals to sign to say they consent.Hope it helpDr.Zahid From: huraira2002@...Date: Fri, 30 Dec 2011 16:58:21 +0000Subject: Consent I can't find explicit consent anywhere can someone shed som light pls? What is it? And when do we need it(what situations)Sent from my BlackBerry wireless device from MTNFrom: "drbaghyarani" <drbaghyarani@...> Sender: Date: Fri, 30 Dec 2011 14:23:27 -0000< >Reply Subject: Regarding and Hi friends I ve recently started from Anatomy. What are all the chapters do we need in and ? Shall i go through the developmental anatomy in this book or any other book? Any questions from thorax? Please guide me... any help will be much appreciated. Thanks and regards Rani Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2012 Report Share Posted January 19, 2012 HiCould anyone please help me with the following questionWhich of the following needs explicit consent?a. to share info with insurance companyb. to share info with other doctors in practicec. to share info with therapist treating the patientd. to share info with patient's GMPI think its b but i'm not sure, could anyone help please?Sid From: Zahid Ahmad <zahiddentalsurgeon@...> Sent: Friday, 30 December 2011, 21:18 Subject: RE: Consent Explicit Consent is taken for survey ,study or resarch purpose for the use of collected data only:To use personal data lawfully you must comply with all UK laws, and meet one condition from the list of conditions set out in the data Protection Act. To use sensitive personal data you must also meet one condition from the additional list of conditions. The conditions that are most likely to apply for research using any personal data are:You have obtained consent from the data subject.You are processing personal data for the legitimate interests of the Organisation or a third party and your use does not cause unwarranted prejudice to the rights and freedoms, or the legitimate interests of the data subject.The conditions that are most likely to apply for research using sensitive personal data are:You have obtained “explicit consent” from the data subject. Explicit consent must be freely given, specific and informed; see below for guidance on obtaining explicit consent.You are carrying out medical research and you are a health professional or someone who owes a similar duty of confidentiality (for example a scientist employed by a health service body). If you choose this condition you will also need to take into account medical ethics and confidentiality constrainYou are analysing racial /ethnic origins for equal opportunities purposes.Your processing of sensitive personal data “is in the substantial public interest and is necessary for research purposes and does not support measures with respect to the particular data subject except with their specific consent nor cause or be likely to cause substantial damage and distress” (The Data Protection (Processing of Sensitive Personal Data) Order 2000). For example, the transmission of relevant patient files by hospitals to local authority cancer registries is in the substantial public interest, because it is vital in protecting and enhancing the public health. If you think that your research may be in the substantial public interest you should include a statement in your initiation document (or equivalent) indicating the potential benefits to the public of your research. However, the substantial public interest is a very high test so you should only use this condition with caution.In most cases where you are using sensitive personal data you will use the explicit consent condition. For consent to be explicit individuals must have a full understanding of what you intend to do with their data and they must “opt-in”; you cannot ask them to opt-out if they object. You should keep a record that you have received explicit consent from the individual whose data you are using. The method you chose to use to collect explicit consent will depend upon the nature of your research but you may choose to:Ask individuals to sign a consent form..If you are asking individuals to complete a questionnaire you may decide to include a data protection statement within the questionnaire and ask individuals to sign to say they consent.Hope it helpDr.Zahid From: huraira2002@...Date: Fri, 30 Dec 2011 16:58:21 +0000Subject: Consent I can't find explicit consent anywhere can someone shed som light pls? What is it? And when do we need it(what situations) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2012 Report Share Posted January 19, 2012 I think It's ABalsamSent from my iPadOn 19 Jan 2012, at 14:28, Sidrah Tul Muntaha <sidrah26@...> wrote: HiCould anyone please help me with the following questionWhich of the following needs explicit consent?a. to share info with insurance companyb. to share info with other doctors in practicec. to share info with therapist treating the patientd. to share info with patient's GMPI think its b but i'm not sure, could anyone help please?Sid From: Zahid Ahmad <zahiddentalsurgeon@...> Sent: Friday, 30 December 2011, 21:18 Subject: RE: Consent Explicit Consent is taken for survey ,study or resarch purpose for the use of collected data only:To use personal data lawfully you must comply with all UK laws, and meet one condition from the list of conditions set out in the data Protection Act. To use sensitive personal data you must also meet one condition from the additional list of conditions. The conditions that are most likely to apply for research using any personal data are:You have obtained consent from the data subject.You are processing personal data for the legitimate interests of the Organisation or a third party and your use does not cause unwarranted prejudice to the rights and freedoms, or the legitimate interests of the data subject.The conditions that are most likely to apply for research using sensitive personal data are:You have obtained “explicit consent†from the data subject. Explicit consent must be freely given, specific and informed; see below for guidance on obtaining explicit consent.You are carrying out medical research and you are a health professional or someone who owes a similar duty of confidentiality (for example a scientist employed by a health service body). If you choose this condition you will also need to take into account medical ethics and confidentiality constrainYou are analysing racial /ethnic origins for equal opportunities purposes.Your processing of sensitive personal data “is in the substantial public interest and is necessary for research purposes and does not support measures with respect to the particular data subject except with their specific consent nor cause or be likely to cause substantial damage and distress†(The Data Protection (Processing of Sensitive Personal Data) Order 2000). For example, the transmission of relevant patient files by hospitals to local authority cancer registries is in the substantial public interest, because it is vital in protecting and enhancing the public health. If you think that your research may be in the substantial public interest you should include a statement in your initiation document (or equivalent) indicating the potential benefits to the public of your research. However, the substantial public interest is a very high test so you should only use this condition with caution.In most cases where you are using sensitive personal data you will use the explicit consent condition. For consent to be explicit individuals must have a full understanding of what you intend to do with their data and they must “opt-inâ€; you cannot ask them to opt-out if they object. You should keep a record that you have received explicit consent from the individual whose data you are using. The method you chose to use to collect explicit consent will depend upon the nature of your research but you may choose to:Ask individuals to sign a consent form..If you are asking individuals to complete a questionnaire you may decide to include a data protection statement within the questionnaire and ask individuals to sign to say they consent.Hope it helpDr.Zahid From: huraira2002@...Date: Fri, 30 Dec 2011 16:58:21 +0000Subject: Consent I can't find explicit consent anywhere can someone shed som light pls? What is it? And when do we need it(what situations) Quote Link to comment Share on other sites More sharing options...
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