How to Use Tables and Figures in Scientific Manuscripts Effectively
Well-designed tables and figures:
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Medical Writing and Study Documentation
How to Deal with Peer Reviewer Comments in Scientific Manuscript Submissions
Peer reviewers are subject-matter experts who evaluate a manuscript’s quality, clarity, novelty, and scientific integrity. Their feedback may highlight:
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Choosing Between Open Access and Subscription-Based Journals: A Clinical Writing Guide
Choose a subscription-based journal if:
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Plagiarism Checks and Language Editing Services in Clinical Manuscript Writing
Plagiarism is the unauthorized use or close imitation of existing text without appropriate citation. In medical writing, it can involve:
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Top Reference Management Tools for Medical Writers in Pharma
Improper or inconsistent citations can lead to:
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How to Write the Discussion and Conclusion Sections in Clinical Manuscripts
The discussion is where your data speaks. It is not a repetition of the results section but a critical interpretation of findings. According to EMA standards and journal guidelines, your discussion should address the following:
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Understanding CTD Modules for Regulatory Submissions in Pharma
The CTD is a standardized format for drug registration applications and comprises five major modules. It was created to simplify and unify the regulatory review process across agencies such as USFDA, EMA, Health Canada, and others.
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How to Prepare Module 2 Summaries for Regulatory Agencies
Module 2 summarizes the essential aspects of your application dossier, including quality, nonclinical, and clinical components. It should highlight key findings, justify decisions, and direct assessors to detailed data found in Modules 3–5.
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eCTD Compilation and Technical Requirements: A Complete Guide
eCTD is based on the Common Technical Document (CTD) format developed by ICH and comprises five main modules:
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Global Dossier Preparation for FDA, EMA, and PMDA: Step-by-Step Guide
The ICH CTD structure consists of five standardized modules:
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