Clinical Trials Overview

The content focuses on various aspects of clinical trials, including study design, methodology, safety evaluations, and ethical considerations. Topics cover both the fundamental principles of conducting trials and specific interventions, such as drug repurposing and the use of novel therapies. The collection highlights regulatory frameworks, challenges in clinical research, and the impacts of trial results on patient care and treatment advancements, underscoring the importance of transparency, data integrity, and adherence to standards throughout the trial process.

clinical trial protocol.pptx of thevpharma
Drug_Development_Phase_I_to_IV_Slides.pptx
compensation rules for clinical trial-related injury and death - Dr Jigar Savaliya.pdf
N-of-1 Clinical trial designs and RCT.pptx
USFDA guide line Drug regulatory affairs
DATOPOTAMAB IN EARLY STAGE BREAST CANCER: MULTIPLE ASSIGNMENT RANDOMIZED I-SPY2 TRIAL.pptx
Schedule of Development of Toxicity testing.pptx
Clinical trial design (randomized, blinded &crossover)
Clinical Trials & its Regulations (Pharmaceutical Regulatory Affairs)
PHASE 1 protocol.pptx by dr Saurabh maurya
Introduction to Good Clinical Practice (GCP)
Clinical trial protocol development Seminar.pdf
“Efficacy of Plantago Major Homoeopathic Mother Tincture as mouth wash with Chlorhexidine (0.2%) mouth wash in management of gingivitis amongst students- A Double Blind, Parallel group, Randomized Control Trial”.pptx
Developing clinical trail protocols.pptx
schedule Y .pptx
8 Effective Patient Recruitment Strategies in Clinical Trials
An ethics committee is a body responsible for reviewing and approving research proposals, ensuring ethical conduct, and protecting the rights, safety, and well-being of research participants
Artificial Intelligence in Health: Success and Challenges
FINEARTS-HF : Finerenone Trial to Investigate Efficacy and Safety Superior to Placebo in Patients with Heart Failure
INVESTIGATIONAL NEW DRUG (IND) for M. Pharm graduate g