Preparation, source data verification, patient safety, investigational product, reporting, and follow-up: the complete process of an ARC monitoring visit.
What does an ARC do during a monitoring visit? Read more »
First drafts, hallucinations, confidentiality, EMA and ICMJE guidelines: how to integrate generative AI into medical writing without compromising quality or compliance.
Medical Writing and Generative AI: What Are the Limits and Best Practices? Read more »
PICO question, study selection, PRISMA 2020, meta-analysis: the methodology for conducting a robust systematic literature review for clinical evaluation.
Systematic Literature Review: How to Conduct One for a Clinical Evaluation Read more »
Content required by ICH E6(R3), Reference Safety Information (RSI), annual update: key information in a clinical trial investigator’s brochure.
Investigator Brochure: Content, Updates, and Best Practices Read more »
Synopsis, 16-section structure, data sources, signature, and submission to CTIS: the steps for drafting a clinical study report in accordance with ICH E3.
Clinical Study Report (CSR): Writing in Accordance with ICH Read more »
Continuing education and eco-responsibility: how developing the skills of clinical teams reduces carbon footprint and turnover.
Pharmacovigilance in Clinical Trials: The Sponsor's Responsibilities Read more »
Biostatistics transforms raw data into robust clinical evidence. Discover its role in study design, data analysis, and benefit/risk assessment of medical devices.
The importance of biostatistics in clinical research Read more »
Continuing education and eco-responsibility: how developing the skills of clinical teams reduces carbon footprint and turnover.
Continuing education: a lever for eco-responsibility in healthcare Read more »
Biomedical research has a significant CO2e footprint. MultiHealth presents concrete recommendations for decarbonizing your clinical trials.
Biomedical research and climate: things are heating up! Read more »
Decentralized SCAC: how digital tools improve real-world clinical data collection for medical devices.
SCAC: decentralization for better representation Read more »
