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Pratik Kapase
Bachlor of pharmacy || Master of pharmacy || Pharmaceutical chemistry || Clinical Research || SAS || Clinical SAS ||
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"Excited to share my latest achievement!I've completed the "Introduction to Clinical Research" course with a score of 94%!This comprehensive course covered essential topics in clinical research, including:Clinical research fundamentalsResearch ethics and informed consentStudy designs (cohort, case-control, cross-sectional, clinical trials)Maintaining high ethical standards, data quality, and uniformity in studiesI'm thrilled to have gained a deeper understanding of clinical research principles and practices. This knowledge will help me contribute to the development of new treatments and therapies, ultimately improving patient outcomes!#ClinicalResearch #ResearchEthics #StudyDesigns #DataQuality #PatientSafety #MedicalResearch"
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Dr. Neil Patel
Resident Doctor of Medicine (M.D.) with Pharmacology in focus.
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I've obtained my certification in "Design and Conduct of Clinical Trials" from Johns Hopkins University I've gained thorough knowledge of Randomization, Blinding, Trial Phases and Designs, Informed Consent Forms, Outcomes, Ethical Considerations, Recruitments and RetentionI'm looking forward to apply these learnings on my currently ongoing Thesis Project which is a Randomized Control Trial and hopefully in my future projects as a Clinical Researcher as well! #clinicaltrails #clinicaloperations #drugdevelopment #research
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Laveena Makhija
Attended Dr. Babasaheb Ambedkar Technological University
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one more course completedCourse :- Introduction to Clinical Research
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Erick Espinosa
Bioanalytical Scientist | IRB member | Clinical research | PK/PD | BA/BE | Clinical trials
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Upholding Ethical Standards in Clinical Research: Insights from an IRB Member.Have you ever wondered about the people behind the scenes who ensure the protection of human subjects in biomedical and behavioral research studies? Meet the Institutional Review Board (IRB), a diverse, interdisciplinary, and autonomous group responsible for evaluating and providing opinions on research protocols involving human subjects. As an IRB member, I am part of a team entrusted with the responsibility of reviewing and monitoring research studies to ensure the protection of the rights and welfare of research participants. Our key functions include assessing the scientific validity and ethical acceptability of proposed studies, minimizing risks to participants, and ensuring compliance with all applicable laws and regulations. We also conduct ongoing reviews of approved studies to ensure compliance with initial terms until completion. Our work relies heavily on collaboration with researchers, participants, and regulatory bodies to foster a research environment that respects participant rights and ensures data integrity and validity. As we continue to navigate the complexities of clinical research, the role of the IRB is more critical than ever in upholding ethical standards and protecting human subjects.
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Deepalaxmi Rathakrishnan
Clinical Research Associate at Hindu Mission Hospital
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Grab this opportunity to know about the basic guidelines (ICH-GCP & E6R2) in clinical research😇
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Sambhav Sharma
Registered Pharmacist |Pursuing Masters in Pharmacy (Pharmaceutics) at Lovely Professional University
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“Excited to share that I’ve successfully completed the ICH Good Clinical Practice and Biomedical Ethics in Health Research course issued by Centre for Professional Enhancement, Lovely Professional University! This comprehensive program equipped me with essential knowledge on research protocol design, ethical review processes, and responsible conduct of research. Looking forward to applying these principles in my work! #ClinicalResearch #EthicsInHealthResearch
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Vishweshwari Chauhan
M.Pharm(Pharmaceutics) | GPAT & NIPER Qualified
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I recently completed e-course on clinical research. I gained the knowledge of:-*The basic concepts of clinical research e.g. what it is, how it differs from standard care and why it is undertaken.*The purpose of ethics in research, what informed consent is and why it is necessary.*Five of the most commonly used study designs how high ethical standards, data quality and uniformity are maintained in a study.
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Rahul Pillai
Eager B.Pharm Graduate | Transitioning to Clinical Data Management Through Data Science
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Excited to share that I’ve completed a course in Clinical Research! 🌟Throughout the course, I gained valuable insights into key areas such as:- The fundamental differences between clinical research and standard care- The ethical principles that guide research, including informed consent- Various study designs, including cohort studies, case control studies, and clinical trials- The importance of maintaining high ethical standards and data qualityThis experience has deepened my understanding of why clinical research is essential, the benefits and risks for participants, and the critical role ethics play in advancing medical knowledge.I look forward to applying these insights in my professional journey!#ClinicalResearch #ProfessionalDevelopment #Ethics #InformedConsent #Healthcare
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Dan Sfera
I meme therefore I am
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In between two degree choices, which is best to enter clinical research
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Vincent Ambale
Data story teller.
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A very fruitful moment for me. I was able to complete a certificate in Social and Behavioral Best practices for Clinical Research.In designing a study, You need to address the followin.1) A well developed Research protocol. 2) Recruitment and Retention of participants.3) Informed Consent Communication.4) Privacy and Confidentiality.5) Study operations.6) Quality Control and Assurance.
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