Webinars>>Clinical Study
How to Create an Electronic Informed Consent​

Embark on an illuminating journey into the realm of electronic informed consent with our exclusive seminar, "Mastering the Art of Electronic Informed Consent Creation." Dive deep into the intricate nuances of regulatory compliance and participant comprehension, ensuring the integrity of your research endeavors and the sanctity of voluntary participation.

Why Should I Attend?

In this enlightening webinar, we'll dissect the pivotal components indispensable for a robust electronic informed consent form:
  1. Comprehensive Participant Profiling: Delve into the meticulous collection of participant data, including intricate details such as demographic information, medical history, and pertinent identifiers. Forge a holistic understanding of each participant's profile, essential for personalized engagement and risk assessment.
  2. Precision in Purpose Articulation: Illuminate the underlying objectives and scientific rationale driving your study or research endeavor. Hone the art of articulating complex concepts with clarity and precision, ensuring participants grasp the significance of their involvement.
  3. Procedural Transparency: Navigate the labyrinth of procedural intricacies by delineating the experimental protocols, intervention modalities, and anticipated outcomes. Provide participants with a comprehensive roadmap, fostering informed decision-making and mitigating uncertainties.
  4. Volitional Commitment Affirmation: Emphasize the voluntariness of participation and the inviolable right to withdraw consent at any juncture without prejudice. Cultivate a culture of autonomy and respect, essential for ethical research conduct and participant welfare.
  5. Risk Stratification and Disclosure: Navigate the terrain of risk assessment with finesse, elucidating potential hazards, adverse events, and mitigation strategies. Strike a delicate balance between transparency and reassurance, empowering participants with the knowledge to navigate inherent uncertainties.
  6. Financial Transparency and Indemnification: Ensure unequivocal clarity regarding financial considerations, reimbursement mechanisms, and indemnification protocols. Uphold the principles of equity and fairness, mitigating financial barriers and fostering trust in research integrity.
  7. Confidentiality Covenant: Safeguard participant confidentiality with unwavering commitment, delineating stringent data protection measures and access protocols. Instill confidence in research governance and data stewardship, vital for fostering participant trust and engagement.
  8. Regulatory Compliance and Legal Adherence: Navigate the intricate web of regulatory requirements with meticulous attention to detail, incorporating essential legal disclosures and compliance mandates. Safeguard research integrity and uphold ethical standards through comprehensive regulatory adherence.

Beyond the rudiments, we'll equip you with advanced methodologies and best practices to craft dynamic, user-centric consent forms tailored to diverse participant demographics and research modalities.
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Embark on a transformative journey toward ethical research conduct and participant-centricity. Enroll now and unlock the boundless potential of electronic informed consent in advancing scientific inquiry and safeguarding participant welfare.
                                                                                                                                                                                    Click Here to Register
Who will benefit: 
  • Regulatory affairs professionals
  • Clinical Research Professionals
  • Principal Investigators
  • Site Managers and Research Coordinators
  • Contract Research Organizations (CROs) Staffs
  • Institutional Review Board (IRB) Members
  • Drug discovery and development professionals (R&D and CMC)
  • Clinical trial managers 
  • Project Managers and Clinical trial specialists
  • Pharmaceutical and Biotech Industry Professionals involved in clinical trial planning and execution.
Date: October 11, 2024
Time: 12 PM EST
​Duration: 60 Minutes

Speaker Mukesh Kumar
​PhD, RAC | CEO, FDAMap

    For more info, fill the box below. We will contact you within 24 hrs.
For additional information on this webinar topic, please call 410-501-5777 or email: [email protected]