Analysis of Drugs (Pharmaceutical Chemistry) - 3 Month Internship Training Program
Join 3 Month Analysis of Drugs (Pharmaceutical Chemistry) Internship Training Program at NextVision Infotech. Master pharmaceutical analysis, instrumental methods, method validation, QC, GLP, research. ₹999 only with certificate.
Program Description
Skills You'll Learn
Projects You'll Work On
Complete Analysis of Drugs (Pharmaceutical Chemistry) Project (3 Month)
Students will complete an advanced drug analysis project including qualitative analysis, quantitative analysis, titrimetric methods, UV-Visible spectroscopy, IR spectroscopy, TLC analysis, HPLC analysis, method development, method validation, stability study, research report, and complete project documentation as per pharmacopoeial standards and ICH guidelines.
Program Modules
W1-2: Weeks 1-2: Pharmaceutical Analysis Fundamentals and Qualitative Analysis
Introduction to pharmaceutical analysis, importance of drug analysis, types of pharmaceutical analysis, 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.
W3-4: Weeks 3-4: 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).
W5-6: Weeks 5-6: 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, atomic absorption spectroscopy (AAS), flame photometry, fluorescence spectroscopy, phosphorescence spectroscopy, polarimetry, refractometry, conductometry, potentiometry.
W7-8: Weeks 7-8: Chromatography, Method Development, and Validation
Chromatography fundamentals, paper chromatography, thin layer chromatography (TLC), TLC plate preparation, TLC development, TLC detection, Rf value, column chromatography, high performance liquid chromatography (HPLC), HPLC instrumentation, HPLC columns, HPLC detectors, HPLC method development, HPLC method validation, gas chromatography (GC), GC instrumentation, GC columns, GC detectors, GC analysis, hyphenated techniques - LC-MS, GC-MS, LC-NMR, method development fundamentals, analytical method development, method optimization, method validation parameters - accuracy, precision, specificity, linearity, range, detection limit, quantitation limit, robustness, ICH guidelines, validation protocol, validation report.
W9-10: Weeks 9-10: Quality Control, Quality Assurance, GLP, and Research
Quality control fundamentals, QC in pharmaceutical industry, QC laboratory, QC testing, QC documentation, quality assurance, QA in pharmaceutical industry, QA systems, QA audits, good manufacturing practices (GMP), good laboratory practices (GLP), laboratory safety, data integrity, documentation, standard operating procedures (SOPs), out of specification (OOS), out of trend (OOT), deviation management, change control, CAPA (Corrective and Preventive Actions), stability testing, stability studies, shelf life, forced degradation studies, research methodology, research design, literature review, data collection, data analysis, research report writing, paper writing, publication.
W11-12: Weeks 11-12: Live Projects, Research, and Certification
Live projects - drug sample analysis, UV-Visible analysis, IR analysis, TLC analysis, HPLC analysis, method development, method validation, stability study, complete documentation, research report, resume building, interview preparation, portfolio building, LinkedIn optimization, viva-voce examination, feedback session, certificate distribution.
Key Features
What You'll Learn
Examination Details
| Exam Name | Full Marks | Pass Marks |
|---|---|---|
| Module-wise Assessment | 100 | 40 |
| Project Evaluation | 100 | 50 |
| Research Report | 100 | 50 |
| Final Presentation | 50 | 25 |
| Viva-Voce | 50 | 25 |
Internship Details
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 advanced pharmaceutical analysis and research
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 advanced practical training
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