BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//IBSAL - ECPv6.18.4//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:IBSAL
X-ORIGINAL-URL:https://ibsal.es/en/
X-WR-CALDESC:Events for IBSAL
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:UTC
BEGIN:STANDARD
TZOFFSETFROM:+0000
TZOFFSETTO:+0000
TZNAME:UTC
DTSTART:20250101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;VALUE=DATE:20261214
DTEND;VALUE=DATE:20261222
DTSTAMP:20261112T133710Z
CREATED:20261112T133631Z
LAST-MODIFIED:20261112T133710Z
UID:29510-1797206400-1797897599@ibsal.es
SUMMARY:Good Clinical Practice (GCP) Guidelines (2026)
DESCRIPTION:Good Clinical Practice (GCP) Guidelines (2026) \nObjective: \nThe overall objective of the course is to train participants in clinical trials on the various aspects of GCP based on the ICH E6 (R3) document on Good Clinical Practice (International Conference on Harmonization). In addition\, it aims to train and update researchers on current regulations in Spain and on the ethical aspects related to the conduct of clinical trials. \n  \nSpecific objectives: \n\nTo deepen understanding of the ethical and legal aspects of clinical research involving drugs and/or medical devices.\nGain a deeper understanding of the Guidelines for Good Clinical Practice\nTo deepen understanding of informed consent in healthcare research\nTo deepen understanding of the responsibilities of the parties involved in clinical research.\nTo deepen understanding of the role of the Institutional Review Board (IRB) in clinical research.\nTo deepen understanding of the essential documentation for clinical trials.\nReinforce the concepts of pharmacovigilance and applicable regulations in clinical trials.\nTo develop the general principles of Good Clinical Practice in Advanced Therapies.\nDeepen understanding of clinical trial audits and inspections.\nRaise awareness of the importance of the Case Report Form in clinical trials.\n\n  \nDate: \nThe exam will be available from December 14 to 21\, 2026\, via the IBSAL platform. \n  \nLocation: \nOnline. IBSAL Platform \nSpeakers: \n\nMs. Carmen Arias De La Fuente.\n\nPh.D. in Molecular Biology. Head of the Clinical Trials Division at the IBSAL Management Unit. \n\nMs. Esperanza López Franco.\n\nPh.D. in Molecular Microbiology and Genetics. Manager and CRA at the UICEC IBSAL/SCReN. \n\nMr. Ricardo López Pérez.\n\nPh.D. in Biochemistry. Manager and CRA at the UICEC IBSAL/SCReN. \n\nMs. Maria Concepcion Turrión Gómez. \n\nPh.D. in Pharmacy and Biochemistry. Technical Secretary of the CEIm for the Salamanca Health District. \n\nMr. José V. Hernández Madrid.\n\nBachelor’s Degree in Pharmacy. Study Coordinator/Data Manager in the Clinical Trials Division at IBSAL. \n\nMs. Cristina Lugones Sánchez. \n\nPh.D. in Nursing. Researcher at IBSAL and APISAL \n\nMs. María Fátima Macho Sánchez-Simón. \n\nBachelor of Veterinary Medicine\, Ph.D. in Neuroscience\, Research Associate at the UICEC’s SCReN at IBSAL. \n  \nProgram: \nOpen document: https://drive.google.com/file/d/12KmWoVesPUekAzsZ6cVEB_Wb9q-suzhE/view?usp=sharing \n  \nRegistration: \nThe pre-registration deadline is Thursday\, December 10\, 2026. Please register individually through our website: \nIn order to successfully complete the course and receive the relevant certificate\, it is necessary to complete 80% of the total program. \nPlease note that you will only be considered enrolled in the course once you receive the confirmation email\, as there is a limit of 40 spots for Ibsal staff. \n  \nMethod of selection: \nEnrollment in the course will be carried out in strict order of enrollment (in courses with high demand\, preference will be given to IBSAL personnel)\, according to the agreement of the IBSAL Training Commission. \n  \n 
URL:https://ibsal.es/en/evento/good-clinical-practice-gcp-guidelines-2026/
LOCATION:Online\, Online
CATEGORIES:IBSAL Course
END:VEVENT
END:VCALENDAR