PDF-Guidance on Research FollowUp
Author : fiona | Published Date : 2021-09-25
Defining a followup period is important to the research protocol even if the followup period is until progression or until death Specify how subjects will be followed
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Guidance on Research FollowUp: Transcript
Defining a followup period is important to the research protocol even if the followup period is until progression or until death Specify how subjects will be followed for assessment of treatmentre. Comments and suggestions regarding this draft document should be submitted within 60 days of publication in the Federal Register of the notice announcing the availability of the draft guidance Submit electronic comments to httpwwwregulationsgov Sub 5741157455574535745357445574545746057459573765744157454574445737657459574615744757447574455745957460574495745557454574595737657458574455744757441574585744457449574545744757376574605744857449574595737657444574585744157446574605737657444 Comments and suggestions regarding this draft document should be submitted within 90 days of publication in the Federal Register of the notice announcing the availability of the draft guidance Submit electronic comments to httpwwwregulationsgov Sub Comments and suggestions regarding this draft document should be submitted within 60 days of publication in the Federal Register of the notice announcing the availability of the draft guidance Submit electronic comments on the draft guidance to http Comments and suggestions regarding this draft document should be submitted within 60 calendar days of publication in the Federal Register of the notice announcing the availability of the draft guidance Submit comments to the Division of Dockets Mana Federal Register Federal Register US Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research CDER January 2010 Clinical Medical brPage 2br Guidance for Industry Assessment of Abuse Potential of Dr omments and suggestions regarding this draft document should be submitted within 60 days of publication in the Federal Register of the notice announcing the availability of the draft guidance Submit electronic comments to httpwwwregulationsgov Subm 3 1 Research ethics committee approval3 2 Grounds for objection 4 3 Labelling of medical devices Furthermore paragraph 96 declares that the products covered by this standard are not breastmilk substitutes and shall not be presented as such Manufacturers often describe followup formula as a substitute for whole cows milk and not infant formula N Comments and suggestions regarding this draft docu ment should be submitted within 60 days of publication in the Federal Register of the notice announcing the availability of the draft guidance Submit comments to the Division of Dockets Management H 100 Purpose All circulars 200 101 Applicability All circulars 200 102 Exceptions 110 200 103 Authorities All circulars 200 104 Supersession All circulars 200 105 Effect On Other Issuances Revised 200 106 Agency Implementation Revised 200 107 OMB Resp com Susan Meldrum. Edinburgh Napier University. November 2016. Career guidance in a small group. Career guidance in a small group. Innovate practice. Lead to positive guidance outcomes. Challenge the long term focus of the career guidance sector on the one-to-one approach. Methods of Implementation. Type the name of . your . organization here.. 1. WHERE ARE WE?: . Follow-up and Monitoring . in SHEP’s 4 Steps. 2. 4 Steps. Activities. 1.. Share goal with farmers.. Sensitization .
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