Hello, I'm Yash

Biomedical Science postgraduate with a strong foundation in medical communications, regulatory writing, clinical trials and hands-on clinical experience.

Recent Articles

Unveiling Natural Solutions: Investigating the Antimicrobial Potential of Thyme Oil, Peppermint Oil…

In the fight against the rising threat of antimicrobial resistance (AMR) and multidrug-resistant (MDR) pathogens, our reliance on conventional antibiotics is becoming increasingly problematic. The reality is stark: bacteria are evolving and many antibiotics are failing. This urgency drove my two-month-long postgraduate research project, where I explored the individual and combined antimicrobial properties of thyme oil, peppermint oil and gold ions against Klebsiella pneumoniae — a notorious, opp...

Aspergillosis Simplified: Communicating Complex Science to Everyday People

When I began designing a 2-page brochure on Allergic Bronchopulmonary Aspergillosis (ABPA) as a part of my Postgraduate academic coursework, my goal was not just to present medical information, but to bridge a crucial knowledge gap for the general public. Despite its severity, ABPA remains a relatively unknown condition. I wanted to change that — by designing an informative, visually engaging and accessible brochure that communicates the condition clearly to people without a medical background.A...

Bridging Non-clinical to Clinical: How IBs Translate Preclinical PK/PD into Human Risk Assessments

In the highly regulated and ethically sensitive landscape of drug development, the transition from non-clinical to clinical phases represents a critical juncture. At the heart of this transition is the Investigator’s Brochure (IB), a living document that serves as the scientific backbone for investigators conducting clinical trials. Far from being a mere formality, the IB plays a pivotal role in integrating preclinical pharmacokinetics (PK), pharmacodynamics (PD) and toxicology data into coheren...

A little bit about me.



Hi, I’m Yash - a Biomedical Science graduate with a P.G.Dip. in Clinical Studies, Medical Writing and Data Management. I specialize in regulatory writing, clinical study documentation and translating complex scientific data into clear, accurate content. My goal is to support healthcare and research by creating precise, evidence-based materials for clinicians, researchers and regulatory stakeholders.