| ECRC–EAFO Seminar on Academic Clinical Research in Oncology & Hematology (SACROH–2023) | |||
| DAY 1 (15.07.2023, 09:30—19:00) | |||
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REGISTRATION (08:00—09:30)
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INTRODUCTION
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| 09:30—09:35 | Welcome Address | Matti AAPRO, Switzerland Elena PAROVICHNIKOVA, Russia Somasundaram SUBRAMANIAN, Russia |
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SESSION 01
Why Clinical Research Matters and How to Come Up to Your Own Research Question |
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| 09:35—09:50 | The Role of Clinical Research for the Physicians, Patients and Society | Somasundaram SUBRAMANIAN, Russia | |
| 09:50—10:20 | Sustainable Culture of Conduction Academic Clinical Research in National Research Center of Hematology | Elena PAROVICHNIKOVA, Russia | |
| 10:20—10:25 | Q&A | ||
| 10:25—10:45 | Challenges of Clinical Trials Conduction in Emerging Countries | MAHANTSHETTY Umesh, India | |
| 10:45—10:50 | Q&A | ||
| 10:50—11:05 | COFFEE PAUSE | ||
| 11:05—11:45 | How We Developed the Question and Looked for the Answer. Experience of the N. N. Petrov National Cancer Center Research Team | Alexey PETROV, Russia | |
| 11:45—12:00 | Q&A | ||
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PRESS CONFERENCE WITH PARTICIPATION OF PATIENT ORGANiZATIONS REPRESENTATIVES
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| 12:00—13:00 | Role of Patient Societies in Clinical Research Development | ||
| 13:00—14:00 | LUNCH | ||
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SESSION 02
WORKSHOP on developing Trial Design and Data Management Plan with Biostatistician and Data Scientist |
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| 14:00—14:40 | How to Communicate with a Biostatistician? Masterclass of Statistical Plan Development | Alexander SUVOROV, Russia | |
| 14:40—15:00 | Q&A | ||
| 15:00—15:50 | Overview of Clinical Trial Designs | Alexander SUVOROV, Russia | |
| 15:50—16:00 | Interactive Q&A | ||
| 16:00—16:20 | COFFEE PAUSE | ||
| 16:20—17:00 | How to Collect All Relevant Data During Your Study. Data Management for Clinical Trials | Timur GALIMOV, Russia | |
| 17:00—17:20 | Interactive Q&A | ||
| 17:20—19:00 | Clinical Trial Synopsis Workshop under Guidance of Biostatistician and Data Scientist | ||
| 19:00—20:00 | Dinner | ||
| DAY 2 (16.07.2023, 09:00—19:00) | |||
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SESSION 03
Research Protocol. Key Part of the Clinical Trial |
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| 09:00—10:00 | Study Protocol as a Tool for Effective and Uniform Data Collection | Ekaterina SOROKINA, Russia | |
| 10:00—10:10 | Q&A | ||
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SESSION 04
Some MUSTs before you START. Part I |
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| 10:10—10:30 | Ethics Review in Clinical Research | Evgeny ROGOV, Russia | |
| 10:30—10:40 | Q&A | ||
| 10:40—11:10 | COFFEE PAUSE | ||
| 11:10—11:40 | Regulatory support of a clinical trial: from obtaining permission to submitting a final report | Maria NASSONOVA, Russia | |
| 11:40—11:50 | Q&A | ||
| 11:50—12:10 | Document Management | Syuzanna KIABIYA, Russia | |
| 12:10—12:20 | Q&A | ||
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SESSION 05
Funding of a Clinical Trial |
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| 12:20—12:50 | Clinical Trial Funding Opportunities | Somasundaram SUBRAMANIAN, Russia | |
| 12:50—13:00 | Q&A | ||
| 13:00—14:00 | LUNCH | ||
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SESSION 06
Some MUSTs before you START. Part II |
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| 14:00—14:20 | Quality Assurance in Clinical Trial | Maria ZAITSEVA, Russia | |
| 14:20—14:30 | Q&A | ||
| 14:30—14:50 | Let the Patient Know about Your Trial. Reaching the Patient Community | Natalia RESHETOVA, Russia | |
| 14:50—15:00 | Q&A | ||
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SESSION 07
IIT and RWD/RWE Research in Clinical Practice |
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| 15:00—15:25 | "Know-hows" of Investigator-iniated trials Planning and Conducting | Tatiana GOLDINA, Russia | |
| 15:25—15:30 | Q&A | ||
| 15:30—15:55 | RWD and RWE in Clinical Research | Tatiana GOLDINA, Russia | |
| 15:55—16:00 | Q&A | ||
| 16:00—16:20 | COFFEE PAUSE | ||
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SESSION 08
Problems of Conducting Clinical Trials in the Different Federal Subjects of Russia |
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| 16:20—16:50 | Optimization of the Clinical Trial Organization and Management at the Level of Federal Subjects of Russia | Andrey CHICHERIN, Russia | |
| 16:50—17:00 | Q&A | ||
| 17:00—17:20 | International Сooperation in the Field of Сlinical Research in Eurasian Economic Union Countries | Alexander SOLODOVNIKOV, Russia | |
| 17:20—17:30 | Q&A | ||
| 17:30—17:55 | Assessment of the Possibilities for the Conduct of Multicenter Clinical Trials in the Federal Subjects of Russia | Yuri KOMAROV, Russia | |
| 17:55—18:00 | Q&A | ||
| 18:00—18:20 | COFFEE PAUSE | ||
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SESSION 09
Happy Ending of Every Clinical Trial |
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| 18:20—18:50 | How to Present Your Research Data Efficiently? | Malcolm MOORE, Thailand | |
| 18:50—19:00 | Q&A | ||
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ADJOURN (19:00)
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