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Da: Buchpark, Trebbin, GermaniaBuchpark
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Condizione: Hervorragend. Zustand: Hervorragend | Sprache: Englisch | Produktart: Bücher | The next edition of the practical guide with regard to The Duty for Sponsor Oversight in Clinical Research was prepared to present in more detail the Risk Based Operational Data Review. As outlined in the previous edition of the practical…guide, the definition of a threshold for missing data and or values was not explicit outlined, in the applicable regulatory binding documents, for example the Clinical trials - Regulation EU No 536/2014. This is also applicable for the upper limit or level of acceptance of, for example, protocol deviations, missing values and or values out of rang or missing safety visits. Nevertheless, the underlying regulations as well as reflexion papers and other articles provide the overall guidance, and required information for the determination of relevant protocol deviations, serious breaches and other deviations or issues. These should normally aligned to the defined outcome parameters of a clinical trial. The same applies for the patient safety, data integrity and data protection Therefore, the supplement edition was prepared for proposing a separate risk-based operational review. The aim includes enhancing with the assumed procedure the quality of the data-set as required, for example, the AMNOG procedure in Germany and or accelerated approval.
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Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The next edition of the practical guide with regard to The Duty for Sponsor Oversight in Clinical Research was prepared to present in more detail the Risk Based Operational Data Review. As outlined in the previous edition of the pr…actical guide, the definition of a threshold for missing data and or values was not explicit outlined, in the applicable regulatory binding documents, for example the Clinical trials - Regulation EU No 536/2014. This is also applicable for the upper limit or level of acceptance of, for example, protocol deviations, missing values and or values out of rang or missing safety visits. Nevertheless, the underlying regulations as well as reflexion papers and other articles provide the overall guidance, and required information for the determination of relevant protocol deviations, serious breaches and other deviations or issues. These should normally aligned to the defined outcome parameters of a clinical trial. The same applies for the patient safety, data integrity and data protection Therefore, the supplement edition was prepared for proposing a separate risk-based operational review. The aim includes enhancing with the assumed procedure the quality of the data-set as required, for example, the AMNOG procedure in Germany and or accelerated approval. 60 pp. Englisch.
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Lingua: Inglese
Editore: Bod - Books On Demand, Bod - Books On Demand Jan 2025, 2025
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Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
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Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The next edition of the practical guide with regard to The Duty for Sponsor Oversight in Clinical Research was prepared to present in more detail the Risk Based Operational Data Review. As outlined in the previous edition of the practi…cal guide, the definition of a threshold for missing data and or values was not explicit outlined, in the applicable regulatory binding documents, for example the Clinical trials - Regulation EU No 536/2014. This is also applicable for the upper limit or level of acceptance of, for example, protocol deviations, missing values and or values out of rang or missing safety visits. Nevertheless, the underlying regulations as well as reflexion papers and other articles provide the overall guidance, and required information for the determination of relevant protocol deviations, serious breaches and other deviations or issues. These should normally aligned to the defined outcome parameters of a clinical trial. The same applies for the patient safety, data integrity and data protection Therefore, the supplement edition was prepared for proposing a separate risk-based operational review. The aim includes enhancing with the assumed procedure the quality of the data-set as required, for example, the AMNOG procedure in Germany and or accelerated approval. 60 pp. Englisch.
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
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Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The next edition of the practical guide with regard to The Duty for Sponsor Oversight in Clinical Research was prepared to present in more detail the Risk Based Operational Data Review. As outlined in the previous edition of the practic…al guide, the definition of a threshold for missing data and or values was not explicit outlined, in the applicable regulatory binding documents, for example the Clinical trials - Regulation EU No 536/2014. This is also applicable for the upper limit or level of acceptance of, for example, protocol deviations, missing values and or values out of rang or missing safety visits. Nevertheless, the underlying regulations as well as reflexion papers and other articles provide the overall guidance, and required information for the determination of relevant protocol deviations, serious breaches and other deviations or issues. These should normally aligned to the defined outcome parameters of a clinical trial. The same applies for the patient safety, data integrity and data protection Therefore, the supplement edition was prepared for proposing a separate risk-based operational review.The aim includes enhancing with the assumed procedure the quality of the data-set as required, for example, the AMNOG procedure in Germany and or accelerated approval.
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Da: preigu, Osnabrück, Germaniapreigu
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Taschenbuch. Condizione: Neu. Handbook: The Duty for Sponsor Oversight in Clinical Trials | A Practical Guide: Risk-Based Operational Data Review Supplement to the e-b**k Edition 1 and 2 | Doris Breiner | Taschenbuch | Handbook: The Duty for Sponsor Oversight in Clinical Trials A Practical Guide: Risk-Based Operational Data Revi…ew Supplement to the E-bo**s Edition 1 and 2 | Englisch | 2025 | BoD - Books on Demand | EAN 9783769319224 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu Print on Demand.
