ResearchManager ’s Post

🧬 Ethics is fundamental to clinical research. Ensuring the integrity, safety, and well-being of participants is not just a regulatory requirement — it’s a moral obligation. How do you guarantee that your clinical projects meet the highest ethical standards? As we advance in medical research and innovation, it’s crucial that we remain committed to ethical practices at every stage of the research process. 👉 How do you prioritize ethics in your clinical research projects? Let’s continue to push the boundaries of innovation, while maintaining the trust and safety of those who contribute to progress. For more insights on ethical clinical research and how we can help, visit https://htl-cro.com/ #Ethics #ClinicalResearch #Integrity #Innovation #PatientSafety #RegulatoryCompliance #MedTech #HealthTech #ResearchExcellence #ClinicalTrials #SafetyFirst

Institutional Ethics Committee takes care of rights, safety & wellbeing of Clinical Research participants. It is an independent committee to maintain Ethics, Rules & Regulations, Standard Operating Systems in Clinical Research. Watch complete video on YouTube - https://lnkd.in/gnRqP9ER #EthicsInClinicalResearch #InstitutionalEthicsCommittee #RulesAndRegulations #StandardOperatingSystems #SiteManagementOrganizations #HospitalsInIndia #Hospitals #participants

Institutional Ethics Committee takes care of rights, safety & wellbeing of Clinical Research participants. It is an independent committee to maintain Ethics, Rules & Regulations, Standard Operating Systems in Clinical Research. Watch complete video on YouTube - https://lnkd.in/d8FEDMBA #EthicsInClinicalResearch #InstitutionalEthicsCommittee #RulesAndRegulations #StandardOperatingSystems #SiteManagementOrganizations #HospitalsInIndia #Hospitals #participants

Research Ethics Committees should: ♦ Be transparent in their functioning. ♦ Be independent of the investigators and sponsor. ♦ Take any national laws and regulations as well as applicable international norms and standards into consideration. ♦ Consider and approve substantial amendments to the research. ♦ Have the right to monitor ongoing studies, especially in relation to serious adverse events. ♦ Receive a final report containing a summary of findings and conclusions at the end of the study.

Hello Everyone!! I'm excited to share that I've completed Ethics and Review of Interventional Clinical Research course! This certification enhanced my understanding of ethics, Clinical Research techniques, tools, and best practices. I'm eager to apply these insights to real-world projects and continue growing in the field of Clinical Research. #ClinicalResearch #Ethics #WorldHealthOrganization

Ethics in Health Research: Putting Patient Safety First 🩺 In clinical research, participant safety isn’t just a guideline—it’s a commitment. For professionals dedicated to making a difference, understanding the ethical foundations of health research is critical. Our Global Health Research Ethics course goes beyond theory, focusing on the real-world implications of every decision you make as a clinical research professional. This course empowers you to prioritise participant safety at every stage of the research process, ensuring that your work not only advances science but also respects and protects the individuals who participate. Because at the end of the day, ethics in research isn’t just about following rules; it’s about safeguarding the lives and well-being of those who trust us. Join us in setting the highest standards in clinical research. Learn more and make participant safety your priority. https://lnkd.in/dDRiA2fb #ClinicalResearch #GCPTraining #ProfessionalDevelopment #AffordableEducation #TASKResearchAcademy

What makes #clinicalreseach ethical ? Ethics for the #clinical Research is major factor for every clinical research #professional. Because, it provide insights about the Reduction of #biasness in clinical trial, enhance #safety of #subjects, good quality #clinicalstudyreports (CSR), #compliance of Clinical Research, subject recruitment, #informedconsent and many more...... For more updates, follow Mohd. Aasim Saifi #clinicalresearch #patientsafety #safety #clinicaltrial #clinical #ethics #informedconsent #patient #research #regulatory #regulatoryaffairs

In her latest article, Kamila Novak from KAN Consulting provides intriguing insights into the evolving landscape of IRBs and Independent Ethics Committees in clinical research: https://lnkd.in/esCqfQBb Discover how #5thPort spearheads patient engagement and revolutionizes electronic informed consent, ensuring seamless, secure, and user-friendly interactions for participants in clinical trials – and make those IRB approvals easier - all with an eye towards total compliance: https://lnkd.in/eQb5YH8P

🌟 Excited to Announce My Certification from WHO in Ethics and Review of Interventional Clinical Research! 🌟 I am thrilled to share that I have recently completed a certification from the World Health Organization (WHO) focused on Ethics and Review of Interventional Clinical Research. This certification has equipped me with a deeper understanding of the ethical considerations and regulatory frameworks involved in clinical trials. Here are the key modules I covered: 1. Foundations of Research Ethics - Understanding ethical principles like respect for persons, beneficence, and justice. - Importance of ethical review boards and informed consent. 2. Study Design and Methodology - Designing scientifically rigorous and ethically sound interventional studies. - Assessing the risk-benefit ratio for participants. 3. Role of Research Ethics Committees (RECs) - Ensuring ethical standards are met and local community values are respected. - Reviewing protocols to safeguard participants' rights and well-being. 4. Informed Consent Process - Ensuring clear communication with participants about study objectives, risks, and benefits. - Upholding the autonomy and confidentiality of research subjects. 5. Regulatory and Good Clinical Practice (GCP) Guidelines - Aligning research practices with international standards. - Monitoring compliance to enhance study integrity and participant safety. This certification has strengthened my skills in ethical oversight and clinical research management,and I am excited to apply this knowledge to future projects. If you're interested in discussing clinical research, ethics, or potential collaborations, feel free to connect! 🔗 #ClinicalResearch #EthicsInResearch #WHO #Certification #ResearchEthics #GoodClinicalPractice #LinkedInLearning #ContinuousLearning

🌍 Updated Declaration of Helsinki Released: A Milestone in Medical Ethics On October 19, 2024, the World Medical Association (WMA) introduced the latest version of the Declaration of Helsinki during the 75th WMA General Assembly in Helsinki, Finland. The Declaration of Helsinki is WMA's foremost policy statement, defining ethical principles for medical research involving human subjects. Since its first adoption in 1964, it has guided countless research studies, emphasizing respect for individuals and prioritizing their well-being in clinical trials. Here’s a timeline of its evolution: 📜 1964: Original Declaration 📜 1975: First Amendment 📜 1983: Second Amendment 📜 1989: Third Amendment 📜 1996: Fourth Amendment 📜 2000: Fifth Amendment 📜 2004: Sixth Amendment 📜 2008: Seventh Amendment 📜 2013: Eighth Amendment 📜 2024: Latest Update This latest 2024 update reflects the WMA's continued dedication to ethical standards, aligning with evolving challenges in medical research and technology. As we integrate these new principles, let’s reaffirm our commitment to upholding the highest ethical standards in clinical research. #MedicalEthics #DeclarationOfHelsinki #WMA #ClinicalResearch