Setting up a new clinical trial site can be overwhelming. From infrastructure, staff recruitment, and documentation to ethics approvals and regulatory compliance—each step needs careful planning and execution. That’s where Doclin Clinical Research Services (DoclinCR) comes in. We help you at every stage, making your site fully trial-ready, compliant, and sponsor-friendly. Here’s a step-by-step guide…
Keywords: Ethics Committee, Role of EC, EC approval process 🧭 Introduction: Ethics at the Heart of Clinical Research Every clinical trial is not just a scientific pursuit but also an ethical responsibility. At the center of this responsibility lies the Ethics Committee (EC)—a body established to protect the rights, safety, and well-being of clinical trial…
Keywords: Clinical trials, Case Report Form (CRF), CRF design best practices, Clinical data collection Introduction: Why CRF Design Matters in Clinical Trials A Case Report Form (CRF) is more than just a tool for data entry—it’s the backbone of clinical data collection. A well-designed CRF ensures protocol compliance, accurate data capture, and ultimately supports the…
Keywords: clinical research, clinical research in India, clinical research careers, what is clinical research Every life-saving drug, vaccine, and medical device that we rely on today has passed through a rigorous process known as clinical research. Behind every tablet, injection, or diagnostic tool is a journey of careful planning, data analysis, human involvement, and ethical…
Keywords: clinical trials, phases of clinical trials, clinical trial process, drug development Have you ever wondered how a new medicine reaches your pharmacy shelf? From groundbreaking laboratory research to a life-saving pill in your hand, a drug must pass through an intensive process known as clinical trials. These trials are not a single event but…
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