VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q85936668 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241120235813.0
008 241120nneanz||abbn n and d
035 ‎‡a (WKP)Q85936668‏
024 ‎‡a 0000-0003-2634-0268‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q85936668‏
100 0 ‎‡a জেমস এ স্মিথ‏ ‎‡9 bn‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a James Andrew Smith‏ ‎‡c biomedical researcher at the University of Oxford‏ ‎‡9 en‏
400 0 ‎‡a James A. Smith‏ ‎‡9 it‏
670 ‎‡a Author's 21(st) Century Cures Act: An Act of Cure or Diagnosis?‏
670 ‎‡a Author's A Quantitative Assessment of Factors Affecting the Technological Development and Adoption of Companion Diagnostics‏
670 ‎‡a Author's Bioprocess decision support tool for scalable manufacture of extracellular vesicles.‏
670 ‎‡a Author's Biosecurity in an age of open science‏
670 ‎‡a Author's Cell assisted lipotransfer in breast augmentation and reconstruction: A systematic review of safety, efficacy, use of patient reported outcomes and study quality.‏
670 ‎‡a Author's Conditional Approval Pathways: The "Special" Case of Global Regenerative Medicine Regulation.‏
670 ‎‡a Author's Corrigendum: A Quantitative Assessment of Factors Affecting the Technological Development and Adoption of Companion Diagnostics.‏
670 ‎‡a Author's Establishing good authentication practice (GAP) in secondary care to protect against falsified medicines and improve patient safety‏
670 ‎‡a Author's Evidence of insufficient quality of reporting in patent landscapes in the life sciences.‏
670 ‎‡a Author's Generating iPSCs: translating cell reprogramming science into scalable and robust biomanufacturing strategies.‏
670 ‎‡a Author's Industry ties and evidence in public comments on the FDA framework for modifications to artificial intelligence/machine learning-based medical devices: a cross sectional study‏
670 ‎‡a Author's Potential lifetime quality of life benefits of choroideremia gene therapy: projections from a clinically informed decision model‏
670 ‎‡a Author's Regulatory Considerations for Gene Therapy Products in the US, EU, and Japan.‏
670 ‎‡a Author's Ten simple rules for implementing open and reproducible research practices after attending a training course‏
670 ‎‡a Author's The magnitude and temporal changes of response in the placebo arm of surgical randomized controlled trials: a systematic review and meta-analysis‏
670 ‎‡a Author's The Reporting Items for Patent Landscapes statement‏
909 ‎‡a (orcid) 0000000326340268‏ ‎‡9 1‏
919 ‎‡a quantitativeassessmentoffactorsaffectingthetechnologicaldevelopmentandadoptionofcompaniondiagnostics‏ ‎‡A A Quantitative Assessment of Factors Affecting the Technological Development and Adoption of Companion Diagnostics‏ ‎‡9 1‏
919 ‎‡a 21stcenturycuresactanactofcureordiagnosis‏ ‎‡A 21(st) Century Cures Act: An Act of Cure or Diagnosis?‏ ‎‡9 1‏
919 ‎‡a bioprocessdecisionsupporttoolforscalablemanufactureofextracellularvesicles‏ ‎‡A Bioprocess decision support tool for scalable manufacture of extracellular vesicles.‏ ‎‡9 1‏
919 ‎‡a biosecurityinanageofopenscience‏ ‎‡A Biosecurity in an age of open science‏ ‎‡9 1‏
919 ‎‡a cellassistedlipotransferinbreastaugmentationandreconstructionasystematicreviewofsafetyefficacyuseofpatientreportedoutcomesandstudyquality‏ ‎‡A Cell assisted lipotransfer in breast augmentation and reconstruction: A systematic review of safety, efficacy, use of patient reported outcomes and study quality.‏ ‎‡9 1‏
919 ‎‡a conditionalapprovalpathwaysthespecialcaseofglobalregenerativemedicineregulation‏ ‎‡A Conditional Approval Pathways: The "Special" Case of Global Regenerative Medicine Regulation.‏ ‎‡9 1‏
919 ‎‡a corrigendumaquantitativeassessmentoffactorsaffectingthetechnologicaldevelopmentandadoptionofcompaniondiagnostics‏ ‎‡A Corrigendum: A Quantitative Assessment of Factors Affecting the Technological Development and Adoption of Companion Diagnostics.‏ ‎‡9 1‏
919 ‎‡a establishinggoodauthenticationpracticegapinsecondarycaretoprotectagainstfalsifiedmedicinesandimprovepatientsafety‏ ‎‡A Establishing good authentication practice (GAP) in secondary care to protect against falsified medicines and improve patient safety‏ ‎‡9 1‏
919 ‎‡a evidenceofinsufficientqualityofreportinginpatentlandscapesinthelifesciences‏ ‎‡A Evidence of insufficient quality of reporting in patent landscapes in the life sciences.‏ ‎‡9 1‏
919 ‎‡a generatingipscstranslatingcellreprogrammingscienceintoscalableandrobustbiomanufacturingstrategies‏ ‎‡A Generating iPSCs: translating cell reprogramming science into scalable and robust biomanufacturing strategies.‏ ‎‡9 1‏
919 ‎‡a industrytiesandevidenceinpubliccommentsonthefdaframeworkformodificationstoartificialintelligencemachinelearningbasedmedicaldevicesacrosssectionalstudy‏ ‎‡A Industry ties and evidence in public comments on the FDA framework for modifications to artificial intelligence/machine learning-based medical devices: a cross sectional study‏ ‎‡9 1‏
919 ‎‡a potentiallifetimequalityoflifebenefitsofchoroideremiagenetherapyprojectionsfromaclinicallyinformeddecisionmodel‏ ‎‡A Potential lifetime quality of life benefits of choroideremia gene therapy: projections from a clinically informed decision model‏ ‎‡9 1‏
919 ‎‡a regulatoryconsiderationsforgenetherapyproductsintheuseuandjapan‏ ‎‡A Regulatory Considerations for Gene Therapy Products in the US, EU, and Japan.‏ ‎‡9 1‏
919 ‎‡a 10simplerulesforimplementingopenandreproducibleresearchpracticesafterattendingatrainingcourse‏ ‎‡A Ten simple rules for implementing open and reproducible research practices after attending a training course‏ ‎‡9 1‏
919 ‎‡a magnitudeandtemporalchangesofresponseintheplaceboarmofsurgicalrandomizedcontrolledtrialsasystematicreviewandmetaanalysis‏ ‎‡A The magnitude and temporal changes of response in the placebo arm of surgical randomized controlled trials: a systematic review and meta-analysis‏ ‎‡9 1‏
919 ‎‡a reportingitemsforpatentlandscapesstatement‏ ‎‡A The Reporting Items for Patent Landscapes statement‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
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