1 / 8

UK Medical Experts in Physician Writing, Case Reports & Regulatory Submissions

At Pubrica, we provide tailored Physician Writing Services for clinicians, researchers, and healthcare professionals in the UK. Our goal is to transform your clinical findings into high-quality, publishable content through our expert Scientific Medical Writing Help For Article development, Regulatory compliance support, and evidence-based documentation.<br>https://pubrica.com/services/physician-writing-services/

pubrica3
Download Presentation

UK Medical Experts in Physician Writing, Case Reports & Regulatory Submissions

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. How to Select the Right Study Design Group: pubrica.com Email: sales@pubrica.com

  2. Introduction • Study design determines how data is collected and interpreted. • Impacts reliability, validity, and scientific credibility. • Must align with objectives, resources, and population characteristics. +44 161 394 0786 +91 9884350006 sales@pubrica.com pubrica.com • Copyright © 2025 pubrica

  3. Understanding Study Designs: An Overview • Study designs are categorized as observational or experimental. • Each subtype addresses a specific type of research question. • Selection depends on purpose: • prevalence, risk, outcome, or intervention. +44 161 394 0786 +91 9884350006 sales@pubrica.com pubrica.com • Copyright © 2025 pubrica

  4. Key Criteria to Consider • Match study design to research question: descriptive, analytical, or interventional. • Factor in timeline: point-in-time (cross-sectional) or over time (cohort/RCT). • Resource and ethical constraints influence feasibility and design type. +44 161 394 0786 +91 9884350006 sales@pubrica.com pubrica.com • Copyright © 2025 pubrica

  5. Match the Design with Objectives • Cross-sectional studies are best for prevalence estimation. • Use case-control for retrospective risk analysis. • Apply cohort or RCT for outcome tracking and intervention assessment. +44 161 394 0786 +91 9884350006 sales@pubrica.com pubrica.com • Copyright © 2025 pubrica

  6. Strengths and Limitations • Each design has trade-offs between validity, cost, and bias. • RCTs offer high validity but are resource-intensive. • Observational studies are efficient but vulnerable to bias. +44 161 394 0786 +91 9884350006 sales@pubrica.com pubrica.com • Copyright © 2025 pubrica

  7. Ethical & Reporting Considerations • RCTs need formal approvals; • observational studies raise data privacy concerns. • Adhere to ethical frameworks like Helsinki Declaration and ICMR/NIH. • Use STROBE (observational) or CONSORT (RCT) checklists for reporting. +44 161 394 0786 +91 9884350006 sales@pubrica.com pubrica.com • Copyright © 2025 pubrica

  8. Contact Us UNITED KINGDOM +44 161 394 0786 INDIA +91-9884350006 EMAIL sales@pubrica.com • Copyright © 2025 pubrica

More Related