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Analysis of Drugs (Pharmaceutical Chemistry) - 1 Month Internship Training Program

Join 1 Month Analysis of Drugs (Pharmaceutical Chemistry) Internship Training Program at NextVision Infotech. Learn qualitative analysis, quantitative analysis, titrimetric methods, spectroscopy, chromatography. ₹499 only with certificate.

30 Days
Anywhere in India • Patna • (Offline & Online)
INT-PHARM-DRUG-30D

Program Description

NextVision Infotech presents a comprehensive Analysis of Drugs (Pharmaceutical Chemistry) Internship Training Program spanning 1 month (30 days). This intensive program is designed for students across all disciplines - B.Pharm, M.Pharm, B.Sc. Chemistry, M.Sc. Chemistry, B.Tech Pharmaceutical Technology, and other related streams - who want to build a strong foundation in pharmaceutical drug analysis. The program covers the complete drug analysis lifecycle from fundamentals to practical laboratory techniques. Students will learn pharmaceutical analysis fundamentals, qualitative analysis, quantitative analysis, titrimetric methods, instrumental methods, spectroscopy, chromatography, and pharmacopoeial standards. Over four weeks, the program progresses from fundamentals to practical drug analysis. Week 1 introduces pharmaceutical analysis fundamentals and qualitative analysis. Week 2 covers quantitative analysis and titrimetric methods. Week 3 focuses on instrumental methods and spectroscopy. Week 4 covers chromatography, pharmacopoeial assays, live projects, and certification. The program follows industry-standard workflows used by professional pharmaceutical chemists and quality control analysts across India. Students work on real drug samples, perform laboratory tests, interpret results, and complete documentation as per IP, BP, USP standards. The curriculum draws inspiration from premier pharmacy institutions across India and follows professional pharmaceutical analysis standards used in the pharmaceutical industry. Students gain practical skills that prepare them for careers in pharmaceutical analysis, quality control, and research. This program is delivered both online and offline, allowing students from any state or city across India to enroll and benefit. The institute is ISO 9001:2015 certified, and the internship certificate is accepted by universities, colleges, and companies throughout the country. Upon successful completion, students receive an Internship Certificate, Industrial Training Certificate, Project Completion Certificate, and an Offer Letter. Learning outcomes include mastering pharmaceutical analysis fundamentals, qualitative analysis, quantitative analysis, instrumental methods, chromatography, and pharmacopoeial standards.

Skills You'll Learn

Pharmaceutical Analysis
Drug Analysis
Qualitative Analysis
Quantitative Analysis
Titrimetric Methods
Acid-Base Titration
Redox Titration
Complexometric Titration
UV-Visible Spectroscopy
IR Spectroscopy
FTIR
TLC
HPLC
GC
LC-MS
GC-MS
Pharmacopoeial Standards
IP
BP
USP
Quality Control
GLP

Projects You'll Work On

Complete Analysis of Drugs (Pharmaceutical Chemistry) Project (1 Month)

Students will complete a drug analysis project including qualitative analysis, quantitative analysis, titrimetric methods, UV-Visible spectroscopy, IR spectroscopy, TLC analysis, HPLC analysis, and complete project documentation as per pharmacopoeial standards (IP, BP, USP).

Program Modules

1

W1: Week 1: Pharmaceutical Analysis Fundamentals and Qualitative Analysis

Introduction to pharmaceutical analysis, importance of drug analysis, types of pharmaceutical analysis - qualitative, quantitative, instrumental, pharmacopoeial standards - IP, BP, USP, Ph. Eur., drug standards, drug purity, drug quality, drug stability, drug degradation, analytical chemistry fundamentals, solution preparation, molarity, normality, molality, percentage solutions, buffer solutions, pH and buffers, acid-base concepts, titration fundamentals, indicators, primary standards, secondary standards, qualitative analysis - tests for functional groups, tests for alkaloids, tests for glycosides, tests for steroids, tests for carbohydrates, tests for proteins, tests for vitamins, tests for antibiotics, impurity testing, limit tests - chloride, sulphate, iron, heavy metals, arsenic, colour and clarity tests.

2

W2: Week 2: Quantitative Analysis and Titrimetric Methods

Quantitative analysis fundamentals, titrimetric methods - acid-base titration, redox titration, complexometric titration, precipitation titration, non-aqueous titration, iodometric titration, potentiometric titration, conductometric titration, titrimetric calculations, standardization of titrants, preparation of standard solutions, indicator selection, titration curves, end point detection, equivalence point, blank determination, gravimetric analysis, precipitation gravimetry, volatilization gravimetry, electrogravimetry, thermal analysis, thermogravimetric analysis (TGA), differential thermal analysis (DTA), differential scanning calorimetry (DSC).

3

W3: Week 3: Instrumental Methods and Spectroscopy

Instrumental methods fundamentals, spectroscopy fundamentals, electromagnetic spectrum, absorption spectroscopy, emission spectroscopy, UV-Visible spectroscopy, Beer-Lambert law, instrumentation, calibration curve, quantitative analysis by UV-Visible, UV-Visible method development, IR spectroscopy, FTIR, instrumentation, IR spectra interpretation, functional group identification, NMR basics, NMR spectroscopy, mass spectrometry basics, mass spectrometry, chromatography fundamentals, paper chromatography, thin layer chromatography (TLC), TLC plate preparation, TLC development, TLC detection, Rf value, column chromatography, chromatographic parameters, resolution, efficiency, selectivity.

4

W4: Week 4: Chromatography, Pharmacopoeial Assays, Live Projects, and Certification

High performance liquid chromatography (HPLC), HPLC instrumentation, HPLC columns, HPLC detectors, HPLC method development, HPLC method validation, HPLC analysis, gas chromatography (GC), GC instrumentation, GC columns, GC detectors, GC analysis, hyphenated techniques - LC-MS, GC-MS, LC-NMR, pharmacopoeial assays, assay methods, pharmacopoeial monographs, drug standardisation, quality control, quality assurance, good laboratory practices (GLP), laboratory safety, data integrity, documentation, live projects - drug sample analysis, UV-Visible analysis, TLC analysis, HPLC analysis, complete documentation, viva-voce examination, certificate distribution.

Key Features

30 Days Comprehensive Training
Industry-Standard Curriculum
Live Laboratory Projects
Pharmacopoeial Standards
Instrumental Methods Training
Professional Documentation
ISO 9001:2015 Certified Institute
Offer Letter Provided
Internship Certificate Included
Industrial Training Certificate
Project Report Guidance
Viva-Voce Preparation
Online & Offline Mode
Pan-India Enrollment

What You'll Learn

Master pharmaceutical analysis fundamentals
Perform qualitative drug analysis
Perform quantitative drug analysis
Apply titrimetric methods
Use UV-Visible spectroscopy
Use IR spectroscopy
Use chromatographic techniques
Perform pharmacopoeial assays
Build a professional pharmaceutical portfolio
Prepare for pharmaceutical analysis jobs across India

Examination Details

Exam Name Full Marks Pass Marks
Module-wise Assessment 100 40
Project Evaluation 100 50
Final Presentation 50 25
Viva-Voce 50 25

Internship Details

Duration 30 Days
Location Anywhere in India • Patna • (Offline & Online)
Available Seats 100
Course Code INT-PHARM-DRUG-30D
Apply Now — ₹499

Prerequisites

  • Pursuing or completed B.Pharm/M.Pharm/B.Sc. Chemistry/M.Sc. Chemistry/B.Tech Pharmaceutical Technology
  • Basic knowledge of chemistry
  • Basic knowledge of laboratory techniques
  • Interest in pharmaceutical analysis

Who Can Enroll ?

  • B.Pharm students (1st to 8th semester)
  • M.Pharm students
  • B.Sc. Chemistry students
  • M.Sc. Chemistry students
  • B.Tech Pharmaceutical Technology students
  • Pharmaceutical analysis aspirants
  • Working professionals wanting to upskill
  • Students from all over India seeking practical training

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