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BEGIN:VEVENT
DTSTART;VALUE=DATE:20261117
DTEND;VALUE=DATE:20261118
DTSTAMP:20260907T162232
CREATED:20260903T021748Z
LAST-MODIFIED:20260903T021748Z
UID:2198-1794873600-1794959999@socra.org
SUMMARY:FDA Clinical Trial Requirements Regulations\, Compliance and GCP Conference=
DESCRIPTION:FDA Clinical Trial Requirements Regulations\, Compliance and GCP LIVE Conference- Nov.17-18\nIncludes Multiple Live Events. The next is on 11/17/2026 at 8:30 AM (EST) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nSpeaker(s)\nContents (4)\n\n\n\nThis LIVE symposium is a distinct opportunity for Sponsor-Investigators and key research staff to receive targeted training directly from FDA\, NIH\, and research industry representatives. It will provide insight into the unique dual-role of sponsor-investigators with in-depth coverage of the applicable FDA regulations\, guidelines\, and best practices. Attendees will take away tools for designing and managing quality research studies that will produce accurate and complete data submissions. The two (2) full-day schedule allows for less disruption to clinical practice and continuing education credits (CME/CNE/SOCRA CE) apply. \nPlease contact us with any questions or concerns at education@socra.org. \nPlease book your Hotel Room here: SOCRA FDA LIVE WORKSHOP ROOM RATE \nDates:\nTuesday November 17th and Wednesday November 18th\, 2026. \nTime:\n8:30 am EST to 4:00 pm EST \n*All times in Eastern Standard Time Zone \n Registration:\n\nStandard Rate – Member Fee – $600\nStandard Rate – Non-Member Fee *- $675\n\nContinuing Education Credit:\nSOCRA designates this educational activity for a maximum of 11.75 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 11.75 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. \nAccreditation Statements:\nCME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. \nCNE for Nurses: Society of Clinical Research Associates is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center’s Commission on Accreditation. \nSOCRA Course Series: 700 \nPlease contact us with any \nquestions or concerns at education@socra.org.
URL:https://socra.org/event/fda-clinical-trial-requirements-regulations-compliance-and-gcp-conference-2/
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20261112
DTEND;VALUE=DATE:20261113
DTSTAMP:20260907T162232
CREATED:20260331T235256Z
LAST-MODIFIED:20260903T021519Z
UID:230-1794441600-1794527999@socra.org
SUMMARY:Monitoring & GCP Workshop - Advanced 
DESCRIPTION:Monitoring & GCP Compliance LIVE Workshop: Nov. 12-13\n Includes Multiple Live Events. The next is on 11/12/2026 at 9:15 AM (EST) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nContents (4)\n\n\n\nGoal: To equip clinical research professionals with the knowledge and practical skills needed to effectively conduct and support clinical trial monitoring activities in accordance with Good Clinical Practice (GCP) and regulatory requirements\, ensuring participant safety\, data integrity\, protocol compliance\, and inspection readiness. \nMember Rate: $645.00 \nNon-Member Rate: $695.00 \nObjective: To provide participants with a comprehensive understanding of clinical trial monitoring\, including regulatory requirements\, Good Clinical Practice (GCP) principles\, risk-based monitoring strategies\, and best practices for identifying and managing compliance issues to support high-quality\, inspection-ready clinical research. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives: Upon completion of the workshop\, the attendee should be able to: \n\nUnderstand the purpose of clinical trial monitoring and the regulatory requirements\nApply Good Clinical Practice principles during monitoring activities and monitor prep\nEvaluate participant safety and data integrity through monitoring practices\nDescribe risk-based monitoring approaches\nIdentify\, document\, and manage non-compliance findings\nUtilize monitoring as a key component of inspection readiness and overall quality management\n\nPlease book your Hotel Room here: 2026 SOCRA Project Management & Monitoring/GCP Conferences – Start your reservation \nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/monitoring-gcp-workshop-advanced/
LOCATION:Nashville\, TN
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20261112
DTEND;VALUE=DATE:20261113
DTSTAMP:20260907T162232
CREATED:20260331T235232Z
LAST-MODIFIED:20260903T021419Z
UID:229-1794441600-1794527999@socra.org
SUMMARY:Project/Program Management - Advanced 
DESCRIPTION:Advanced Project/Program Management LIVE Workshop: Nov. 12-13\n Includes Multiple Live Events. The next is on 11/12/2026 at 9:30 AM (EST) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nSpeaker(s)\nContents (4)\n\n\n\nGoal: To equip clinical research professionals with practical project and program management tools and strategies to effectively plan\, execute\, monitor\, and lead research projects while managing risk\, finances\, contracts\, teams\, and stakeholder relationships. \nMember Rate: $645.00 \nNon-Member Rate: $695.00 \nObjective: Provide attendees with the knowledge\, tools\, and practical techniques to apply project management principles to clinical research\, including planning and tracking projects\, mitigating risk\, managing budgets and contracts\,a nd navigating team and organizational dynamics. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives: Upon completion of the workshop\, the attendee should be able to: \n\nApply core project management principles and PMI concepts to the planning\, execution\, monitoring\, and completion of clinical research projects.\nUtilize project management tools and techniques\, including Gantt charts\, SOPs\, flowcharts\, and shared calendars\, to effectively plan\, track\, and assess project progress.\nIdentify and mitigate project risks using practical risk management and risk-avoidance strategies.\nApply effective approaches to study budgeting\, financial tracking\, contract management\, and sponsor-site negotiations throughout the clinical trial lifecycle.\nImplement strategies for managing diverse leadership and organizational styles\, resolving conflict\, strengthening teams\, and improving stakeholder collaboration.\n\nPlease book your Hotel Room here: 2026 SOCRA Project Management & Monitoring/GCP Conferences – Start your reservation \nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/project-program-management-advanced/
LOCATION:Nashville\, TN
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20261028
DTEND;VALUE=DATE:20261029
DTSTAMP:20260907T162232
CREATED:20260331T235208Z
LAST-MODIFIED:20260903T021204Z
UID:228-1793145600-1793231999@socra.org
SUMMARY:CCRP Prep and GCP Review Course 
DESCRIPTION:Clinical Research Professional Certification Preparation and GCP Virtual Review Course – October 28 & 29\, 2026\n Includes Multiple Live Events. The next is on 10/28/2026 at 12:00 PM (EDT) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nSpeaker(s)\nContents (4)\n\n\n\nGoal: The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination. \nThis course will review the concepts identified in the CCRP Certification Examination Content Outline\, as well as the Standards of Practice including the ICH Guidelines and FDA Regulations that govern clinical research practice. \nMember Rate: $295.00 \nNon-Member Rate: $370.00 \nObjective: The goal will be accomplished through lecture\, discussion and practical application facilitated by certified clinical research professionals with combined clinical research experience of more than 20 years. Information will be presented and discussed regarding the conduct of clinical trials; regulatory guidelines regarding IRB oversight and human research protections; ethical issues in clinical research; and workshops will stress the ability to follow directions and practices related to abstracting information and completing case report forms and other records. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives: Upon completion of the workshop\, the attendee should be able to: \n\nDiscuss the basic requirements necessary to meet the demands of a CRP in clinical practice\nDiscuss the basic components of compliance – Law\, regulation\, guidance\, policy and procedure\nExplain the drug/biologic development process\nDescribe the device development process\nOutline concepts for Good Clinical Practice (GCP)\nExplain the elements of informed consent\nDescribe the membership and reporting requirements of IRBs\nExplain rules relating to financial disclosure\nDiscuss the basics of study design\nExplain the rules and reporting requirements for adverse events and serious adverse events\nExplain study closure procedures and record retention guidelines\nOutline the reasons for monitoring\, audits and site visits\nExplain the Food and Drug Administration rules\, regulations\, and guidelines on research\nDiscuss the importance of investigational drug accountability\nDemonstrate and describe how to read clinical reports and records\nDiscuss Quality Assurance including\, Monitoring and Auditing\nExplain issues that would constitute clinical fraud\n\nThe purchase of this course is optional. It is not required to sit for or pass the CCRP certification exam. Purchasing and completing this course will not guarantee a passing score on the CCRP certification examination. \nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course-5/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260924
DTEND;VALUE=DATE:20260925
DTSTAMP:20260907T162232
CREATED:20260331T235130Z
LAST-MODIFIED:20260331T235443Z
UID:227-1790208000-1790294399@socra.org
SUMMARY:2026 SOCRA Annual Conference
DESCRIPTION:Join over 1\,000 of your colleagues at SOCRA’s Annual Conference! Each year\, SOCRA gathers clinical research professionals from around the world. Immerse yourself in this three-day conference filled with current information\, essential tools\, best practices\, and comprehensive training to ensure your clinical research practice remains up-to-date and compliant. The program boasts expert-led academic sessions\, interactive workshops\, ample networking opportunities\, a peer-driven poster session\, and an engaging exhibit program. Don’t miss this chance to connect\, learn\, and stay at the forefront of the industry. Mark your calendar and join us!
URL:https://socra.org/event/2026-socra-annual-conference/
LOCATION:Denver\, CO
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260923
DTEND;VALUE=DATE:20260924
DTSTAMP:20260907T162232
CREATED:20260331T235107Z
LAST-MODIFIED:20260331T235428Z
UID:226-1790121600-1790207999@socra.org
SUMMARY:CCRP Prep and GCP Review Course 
DESCRIPTION:
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course-4/
LOCATION:Denver\, CO
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260923
DTEND;VALUE=DATE:20260924
DTSTAMP:20260907T162232
CREATED:20260331T235044Z
LAST-MODIFIED:20260903T020829Z
UID:225-1790121600-1790207999@socra.org
SUMMARY:SOCRA Digital Health & Clinical Research Workshop
DESCRIPTION:SOCRA Digital Health & Clinical Research Workshop- LIVE\n Includes a Live In-Person Event on 09/23/2026 at 10:00 AM (EDT) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nContents (3)\n\n\n\nGoal: To equip clinical research professionals with the knowledge and practical decision-making skills to responsibly integrate digital health technologies and AI throughout the clinical trial lifecycle while ensuring participant protection\, regulatory compliance\, operational excellence\, and scientific integrity. \nMember Rate: $295.00 \nNon-Member Rate: $370.00 \nPlease book your room here: SOCRA 2026 Annual Conference – Start your reservation \nObjective: To provide participants with a practical framework for evaluating\, implementing\, and governing digital health technologies and AI across the clinical trial lifecycle\, enabling them to make informed decisions that enhance research quality\, operational efficiency\, participant experience\, and regulatory compliance. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives: Upon completion of the workshop\, the attendee should be able to: \n\nEvaluate opportunities to integrate digital health technologies (DHTs)\, artificial intelligence (AI)\, digital biomarkers\, and real-world evidence across the clinical trial lifecycle to improve research quality\, operational efficiency\, and participant experience.\nDevelop practical strategies for designing and operationalizing decentralized and hybrid clinical trials using digital informed consent\, remote participant monitoring\, and participant-centered technologies.\nApply the SMART Framework to evaluate\, implement\, and govern digital innovation throughout the clinical trial lifecycle while balancing operational efficiency\, participant protection\, regulatory compliance\, and scientific integrity.\nApply regulatory\, ethical\, equity\, and governance principles to evaluate digital health and AI solutions\, including regulatory compliance\, bias mitigation\, participant protection\, human oversight\, and responsible implementation.\nDevelop practical approaches to digital data management and governance that support data quality\, privacy\, cybersecurity\, interoperability\, and research integrity throughout the clinical trial lifecycle.\n\nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/socra-digital-health-clinical-research-workshop/
LOCATION:Denver\, CO
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260820T100000
DTEND;TZID=America/New_York:20260820T110000
DTSTAMP:20260907T162232
CREATED:20260814T184534Z
LAST-MODIFIED:20260814T213249Z
UID:1817-1787220000-1787223600@socra.org
SUMMARY:Arkansas Chapter: Dr. Albert Kligman and the Holmesburg Prison Experiments
DESCRIPTION:Learning Objectives \n\nLearn the history behind Dr. Kligman’s experiments.\nDiscuss factors to be considered when conducting research with prisoners.\nExplore misconceptions / miscommunications surrounding informed consent.\nGain a better understanding of how to perform ethical research.\n\nSpeaker: Brandy M. Fox\, PhD
URL:https://socra.org/event/arkansas-chapter-dr-albert-kligman-and-the-holmesburg-prison-experiments/
LOCATION:Virtual 
CATEGORIES:Chapter Event
ORGANIZER;CN="Laura Adkins":MAILTO:lladkins@uams.edu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20260819T110000
DTEND;TZID=UTC:20260819T120000
DTSTAMP:20260907T162232
CREATED:20260814T213724Z
LAST-MODIFIED:20260814T213724Z
UID:1835-1787137200-1787140800@socra.org
SUMMARY:Central Virginia Event: Monitoring :  Oversight with Impact
DESCRIPTION:Learning Objectives \n\nExplain what drives the monitoring process\nExamine monitoring visits\, how to prepare and common findings\nReview practical\, real-world case studies and scenarios along with current monitoring trends seen through the GCP E6(R3) lens\n\nSpeaker: Laura Adkins\, MAP CCRP\, CCRA\, AdvCRS
URL:https://socra.org/event/central-virginia-event-monitoring-oversight-with-impact/
LOCATION:Virtual 
CATEGORIES:Chapter Event
ORGANIZER;CN="Shirley Helm":MAILTO:shirley.helm@vcuhealth.org
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260813
DTEND;VALUE=DATE:20260814
DTSTAMP:20260907T162232
CREATED:20260331T234955Z
LAST-MODIFIED:20260331T235435Z
UID:224-1786579200-1786665599@socra.org
SUMMARY:Quality Management 
DESCRIPTION:This interactive virtual workshop will be facilitated by clinical research professionals with a wealth of industry expertise. The purpose of this workshop is to assist research professionals in understanding\, developing\, and implementing quality management systems (QMS) in the conduct of clinical trials. This conference provides attendees with new information\, tools\, and real life examples to help participants navigate the components of quality management – quality planning\, quality control\, quality assurance\, and quality improvement. \nContinuing Education Credit Hours\nSOCRA designates this educational activity for a maximum of 9.75 Continuing Education Credits for SOCRA CE and Nurse CNE. \nSOCRA designates this live activity for a maximum of 9.75 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. \nAccreditation Statements\nCME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. \nCNE for Nurses: Society of Clinical Research Associates is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center’s Commission on Accreditation. \nSOCRA Course Series: 120
URL:https://socra.org/event/quality-management/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260808
DTEND;VALUE=DATE:20260809
DTSTAMP:20260907T162232
CREATED:20260331T234921Z
LAST-MODIFIED:20260331T235449Z
UID:223-1786147200-1786233599@socra.org
SUMMARY:Site Coordinator Course (include CTMS) 
DESCRIPTION:
URL:https://socra.org/event/site-coordinator-course-include-ctms/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20260730T120000
DTEND;TZID=America/Los_Angeles:20260730T130000
DTSTAMP:20260907T162232
CREATED:20260814T213253Z
LAST-MODIFIED:20260814T213301Z
UID:1830-1785412800-1785416400@socra.org
SUMMARY:San Francisco Bay Chapter: Using AI for Inspectional Readiness: The One Day Pilot or the Routine Inspection
DESCRIPTION:Learning Objectives \n\nExamine how AI can be used to support inspectional readiness for both a one-day pilot inspection or a routing surveillance inspection\nHear real-world perspectives on inspections from using AI in the readiness process.\nExplore the use of AI in responding to FDA\, or other regulatory body\, inspections.\n\nSpeaker: Mr. Eric Pittman
URL:https://socra.org/event/san-francisco-bay-chapter-using-ai-for-inspectional-readiness-the-one-day-pilot-or-the-routine-inspection/
LOCATION:Virtual 
CATEGORIES:Chapter Event
ORGANIZER;CN="Archana Narasanna":MAILTO:socrabayareachapter@gmail.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260708
DTEND;VALUE=DATE:20260709
DTSTAMP:20260907T162232
CREATED:20260331T234819Z
LAST-MODIFIED:20260331T235453Z
UID:222-1783468800-1783555199@socra.org
SUMMARY:Device Research & Regulatory Information
DESCRIPTION:Join us for a medical device webinar series. The program will feature 3 sessions and 3 experts presenting topics to assist those in roles specific to medical device design\, development\, testing\, analysis\, and post market management. \nContinuing Education Credit Hours:\nSOCRA designates this educational activity for a maximum of 3 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 3 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. \n\nAccreditation Statements\nCME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. \nCNE for Nurses: Society of Clinical Research Associates is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center’s Commission on Accreditation.
URL:https://socra.org/event/device-research-regulatory-information/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260616
DTEND;VALUE=DATE:20260617
DTSTAMP:20260907T162232
CREATED:20260331T234601Z
LAST-MODIFIED:20260331T235456Z
UID:221-1781568000-1781654399@socra.org
SUMMARY:CCRP Prep and GCP Review Course
DESCRIPTION:
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course-3/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260609
DTEND;VALUE=DATE:20260610
DTSTAMP:20260907T162232
CREATED:20260331T234439Z
LAST-MODIFIED:20260331T234450Z
UID:220-1780963200-1781049599@socra.org
SUMMARY:Monitoring & GCP Workshop - Beginner
DESCRIPTION:
URL:https://socra.org/event/monitoring-gcp-workshop-beginner/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260520
DTEND;VALUE=DATE:20260522
DTSTAMP:20260907T162232
CREATED:20260331T234349Z
LAST-MODIFIED:20260401T205942Z
UID:219-1779235200-1779407999@socra.org
SUMMARY:Project Management - Beginner 
DESCRIPTION:Goal\nThis introduction to clinical research project management workshop incorporates a broad range of skill sets in order to plan\, administer\, track\, evaluate and report on activities involved clinical research process. The goal of this interactive workshop is to introduce\, affirm\, and enhance the participant’s understanding of project management. \nObjective\nThrough discussion\, presentation\, and interaction\, this virtual program will broaden the participants’ knowledge of the project management art and science. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives\nUpon completion of the workshop\, the attendee should be able to: \n\nDescribe  skills and responsibilities to move from a clinical research coordinator or other research roles to learn about the responsibilities of a Project Manager.\nDefine key terms and concepts associated with Project Management.\nDescribe project management processes following PMI (Project Management Institute) guidelines (initiation\, planning\, execution\, monitoring\, controlling\, and closing).\nDiscuss the processes and procedures that are necessary to develop an infrastructure that will support the various tasks associated with Project Management in Clinical Research.\nDescribe Project Management constraints including Scope\, Time\, Budget\, and Performance.\nLearn about effective strategies in Virtual Project Management and Decentralized Clinical Trials.\nDiscuss basic principles of Risk Management\, Risk Avoidance and Risk Mitigation.\nLearn how Organizational Tools and Techniques can improve effectiveness and maintain quality in project management.\nDiscuss Organizational Dynamics and self-management in project management to promote effective team building.\nDiscuss approaches to work effectively with different leadership styles and organizational cultures.\n\nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/project-management-beginner/
LOCATION:Virtual 
ATTACH;FMTTYPE=image/png:https://socra.org/wp-content/uploads/2026/03/SOCRA_events_featured4-1.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260508
DTEND;VALUE=DATE:20260509
DTSTAMP:20260907T162232
CREATED:20260331T234215Z
LAST-MODIFIED:20260401T205724Z
UID:218-1778198400-1778284799@socra.org
SUMMARY:Pediatric Clinical Trials
DESCRIPTION:This interactive virtual workshop will be facilitated by clinical research professionals with a wealth of industry expertise. The purpose of this workshop is to assist research professionals in improving their skills and their understanding of the responsibilities of conducting clinical research in the pediatric population. This conference provides attendees with new information\, management tools\, and real life examples\, to help participants navigate the evolving landscape of pediatric research. \nContinuing Education Credit Hours\nSOCRA designates this educational activity for a maximum of 6.5 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 6.5 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. \nAccreditation Statements\nCME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. \nCNE for Nurses: Society of Clinical Research Associates is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation. \nSOCRA Course Series: 850
URL:https://socra.org/event/pediatric-clinical-trials/
LOCATION:Virtual 
ATTACH;FMTTYPE=image/png:https://socra.org/wp-content/uploads/2026/03/SOCRA_events_featured2.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260428
DTEND;VALUE=DATE:20260430
DTSTAMP:20260907T162232
CREATED:20260331T233814Z
LAST-MODIFIED:20260401T203613Z
UID:216-1777334400-1777507199@socra.org
SUMMARY:FDA Clinical Trial Requirements Regulations\, Compliance and GCP Conference
DESCRIPTION:This virtual symposium is a distinct opportunity for Sponsor-Investigators and key research staff to receive targeted training directly from FDA\, NIH\, and research industry representatives. It will provide insight into the unique dual-role of sponsor-investigators with in-depth coverage of the applicable FDA regulations\, guidelines\, and best practices. Attendees will take away tools for designing and managing quality research studies that will produce accurate and complete data submissions. The two (2) full-day schedule allows for less disruption to clinical practice and continuing education credits (CME/CNE/SOCRA CE) apply. \nPlease note\, this workshop is intended to be interactive. Video attendance is strongly encouraged. Once you register\, you will be able to install and test the appropriate software to ensure your audio and video will work properly during the program. Please be sure to give yourself time to address any technical issues that might arise. Please contact us with any questions or concerns at education@socra.org. \nContinuing Education Credit Hours:\nSOCRA designates this educational activity for a maximum of 11.75 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 11.75 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. \nAccreditation Statements:\nCME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.\nCNE for Nurses: Society of Clinical Research Associates is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center’s Commission on Accreditation.\nSOCRA Course Series: 700
URL:https://socra.org/event/fda-clinical-trial-requirements-regulations-compliance-and-gcp-conference/
LOCATION:Virtual 
ATTACH;FMTTYPE=image/png:https://socra.org/wp-content/uploads/2026/03/SOCRA_events_featured1.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260422
DTEND;VALUE=DATE:20260424
DTSTAMP:20260907T162232
CREATED:20260331T233432Z
LAST-MODIFIED:20260401T205846Z
UID:214-1776816000-1776988799@socra.org
SUMMARY:CCRP Prep and GCP Review Course
DESCRIPTION:Goal\nThe purpose of this workshop is to assist the participant in preparing for the CCRP certification examination. \nThis course will review the concepts identified in the CCRP Certification Examination Content Outline\, as well as the Standards of Practice including the ICH Guidelines and FDA Regulations that govern clinical research practice. \nObjective\nThe goal will be accomplished through lecture\, discussion and practical application facilitated by certified clinical research professionals with combined clinical research experience of more than 20 years. Information will be presented and discussed regarding the conduct of clinical trials; regulatory guidelines regarding IRB oversight and human research protections; ethical issues in clinical research; and workshops will stress the ability to follow directions and practices related to abstracting information and completing case report forms and other records. \nLearning Objectives\nUpon completion of the workshop\, the attendee should be able to: \nDiscuss the basic requirements necessary to meet the demands of a CRP in clinical practice\nDiscuss the basic components of compliance – Law\, regulation\, guidance\, policy and procedure\nExplain the drug/biologic development process\nDescribe the device development process\nOutline concepts for Good Clinical Practice (GCP)\nExplain the elements of informed consent\nDescribe the membership and reporting requirements of IRBs\nExplain rules relating to financial disclosure\nDiscuss the basics of study design\nExplain the rules and reporting requirements for adverse events and serious adverse events\nExplain study closure procedures and record retention guidelines\nOutline the reasons for monitoring\, audits and site visits\nExplain the Food and Drug Administration rules\, regulations\, and guidelines on research\nDiscuss the importance of investigational drug accountability\nDemonstrate and describe how to read clinical reports and records\nDiscuss Quality Assurance including\, Monitoring and Auditing\nExplain issues that would constitute clinical fraud \nThe purchase of this course is optional. It is not required to sit for or pass the CCRP certification exam. Purchasing and completing this course will not guarantee a passing score on the CCRP certification examination.
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course-2/
LOCATION:Virtual 
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BEGIN:VEVENT
DTSTART;TZID=UTC:20260225T000000
DTEND;TZID=UTC:20260226T000000
DTSTAMP:20260907T162232
CREATED:20260331T232944Z
LAST-MODIFIED:20260331T233837Z
UID:209-1771977600-1772064000@socra.org
SUMMARY:CCRP Prep and GCP Review Course 
DESCRIPTION:
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course/
LOCATION:Virtual 
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END:VCALENDAR