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Clinical Trials - Practical Issues in Labeling the Trial Drugs

The double blind controlled clinical trials are universally accepted as the gold standard for estimating the efficacy of a new treatment in comparison with a standard drug or placebo. Medical community and pharmaceutical industry have been practicing this... Read >

Best Practices in eCRF Designing for Data Collection

The eCRF (electronic Case Report Form) is an Electronic Data Capturing (EDC) tool used in clinical trials to collect protocol required information. A well designed and properly structured eCRF is prerequisite for simplified data collection. eCRF design te... Read >

Site Management Organization - The Future

Introduction Clinical trial is the most time consuming phase in development of any new drug. In order to reduce this time line large numbers of pharmaceutical companies now choose to outsource their clinical trials to a more professional clinical resea... Read >

Regulation Importance in Pharma Industry

Today, Regulatory Affairs is a dynamic business unit that works with a focus to get products to the market with commercially viable label in the least possible time and expenses. In view of the increasing global competitiveness among pharmaceutical compan... Read >