What is it about?

I, Dr. Saumya Pandey Ph.D., constantly endeavor to provide meaningful high-quality research contributions in the competitive women's health research field. Bioethics and written informed consent are core tenets of good practice clinical research globally including States of New York, Nebraska, Texas, USA and Lucknow/Udaipur, India wherein I have invested my female scientific brainpower for cost-effective biomedical research! Clomiphene citrate and fetal safety assessments warrants collaborative research efforts at the population level using cohort-based study designs with retrospective and/or prospective study approaches. Sample size calculations should be adequate for significant study power so as to interpret data-sets reliable with reproducibility.

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Why is it important?

Clomiphene citrate, fetal safety, cohort-based retrospective clinical research studies are warranted to address effectively the growing public health challenge of reproductive disorders in ethnically disparate populations worldwide.

Perspectives

Dissecting the intricacies in reproductive medicine/immunology is essential for diminishing the increasing trends of miscarriages, infertility, etc, in women of child-bearing age; therefore, my public health research oriented publication crisply provides a snapshot of clomiphene citrate and fetal safety in a specific patient population subset. Future replicative studies with pharmacogenetic study approaches are warranted to provide immunomodulatory strategies in cost-effective reproductive health management on a global platform with a pooled sample-set of women of varying genetic landscapes. DR. SAUMYA PANDEY PH.D. DRSAUMYAPANDEY11@GMAIL.COM Lucknow, India (Author Dr. Pandey's hometown); December 28, 2018!

DR. SAUMYA PANDEY

Read the Original

This page is a summary of: Re: The fetal safety of clomiphene citrate: a population based retrospective cohort study, BJOG An International Journal of Obstetrics & Gynaecology, July 2017, Wiley,
DOI: 10.1111/1471-0528.14715.
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