---
title: "Eshpreet Wasan - Pharmaceutical intern in Dehradun | Tal"
description: "Meet Eshpreet Wasan, B.Pharma | Clinical Research & Regulatory Affairs | AI in Pharma Certified | GMP · GCP · Pharmacovigilance | Open to Global Roles based in Dehradun."
image: "https://tal.club/meet/eshpreet/share-image"
---

# Eshpreet Wasan on Tal

## Headline

B\.Pharma \| Clinical Research & Regulatory Affairs \| AI in Pharma Certified \| GMP · GCP · Pharmacovigilance \| Open to Global Roles

## About

I’m Eshpreet — a B\.Pharma graduate from Graphic Era Hill University \(2025\) with a post\-grad clinical research certification and a specialisation in AI in Pharma from the Life Sciences Sector Skill Development Council\. My focus is the intersection of clinical trials, regulatory submissions, and how AI is changing both\. During my internship at Nitin Lifesciences Ltd\. \(a Synokem Pharmaceuticals company\), I got hands\-on exposure to pharmaceutical manufacturing, GMP compliance, QA documentation, and industrial drug production — the kind of ground\-level understanding that classroom training rarely gives you\. My academic projects took me into drug formulation research — developing an oral anti\-ulcer film using catechu — and into reviewing the latest advances in antihypertensive, antidiabetic, and anticancer therapies\. A pharmacovigilance seminar I attended shifted my interest firmly toward drug safety and regulatory systems\. If you work in clinical research, regulatory affairs, pharmacovigilance, or pharma AI — I’d love to connect\. Clinical Research \| Regulatory Affairs \| Pharmacovigilance \| GMP \| GCP \| Drug Development \| AI in Pharma \| Pharmaceutical Sciences \| Regulatory Submissions \| Clinical Trials

## Location

Dehradun

## Work experience

Pharmaceutical intern at Nitin Lifesciences Ltd\. \(Synokem Pharmaceuticals\), Jul 2024 \- Aug 2024 · 2 mos, Paonta Sahib, Himachal Pradesh, India, • Applied GMP principles across pharmaceutical manufacturing and tablet/formulation production lines, observing compliance protocols at each stage • Supported QA documentation processes including batch records, SOPs, and deviation reports in line with regulatory requirements • Assisted in analytical testing and basic research activities under supervision of senior technical staff • Observed end\-to\-end drug production workflow from raw material handling to finished product release, building understanding of industrial\-scale pharma operations\.

## Education

Advance diploma, Clinical Research, Clinogenesis research institute

Bachelor of Pharmacy \- BPharm, Pharmacy, Graphic Era Hill University

[View the original profile](https://tal.club/meet/eshpreet)

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