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PH

Pharmacy

Drug Discovery

Specialization tracks & curriculum

13 industry-oriented internship tracks. Each track has its own detailed curriculum below — pick one when you enroll.

Analytical R&D

Most-demanded analytical lab internship covering HPLC, GC, UV, dissolution and method development.

7 modules
Duration: 8–12 WeeksCore practical: HPLC, GC, UV
Modules
  1. 1Introduction to Analytical R&D
    • Pharma analytical workflow
    • GLP basics
  2. 2Instrumentation
    • HPLC
    • UPLC
    • GC
    • UV Spectroscopy
    • FTIR
  3. 3Practical Training
    • Mobile phase preparation
    • Standard preparation
    • Sample analysis
    • Calibration
  4. 4Method Development
    • Column selection
    • pH optimization
    • Resolution improvement
  5. 5Method Validation
    • Accuracy
    • Precision
    • Specificity
    • Robustness
    • LOD & LOQ
  6. 6Stability Studies
    • Accelerated stability
    • Stability chamber handling
  7. 7Documentation
    • Analytical reports
    • SOP preparation
    • Validation reports
Final Project: HPLC method validation
Quality Assurance (QA)

GMP documentation, audits, CAPA and data integrity inside regulated pharma plants.

7 modules
Core practical: SOPs, CAPABest for: B.Pharm, M.Pharm, Pharm.D
Modules
  1. 1GMP & Documentation
    • cGMP
    • GDP
    • Data integrity
  2. 2SOP Systems
    • SOP drafting
    • Document control
  3. 3Batch Documentation
    • BMR/BPR review
    • Line clearance
  4. 4QA Systems
    • Deviations
    • CAPA
    • Change control
  5. 5Audit Management
    • Internal audits
    • Regulatory inspections
  6. 6Validation Overview
    • Process validation
    • Cleaning validation
  7. 7Practical Exposure
    • QA floor rounds
    • Batch review exercises
Final Project: Deviation & CAPA management
Quality Control (QC)

Raw material, in-process and finished product testing across chemical and microbial QC.

6 modules
Core practical: Wet chemistry
Modules
  1. 1Wet Lab Analysis
    • Assay
    • Titration
    • Identification tests
  2. 2Instrumental Analysis
    • HPLC
    • UV
    • Dissolution
  3. 3Raw Material Testing
    • APIs
    • Excipients
  4. 4Finished Product Testing
    • Tablets
    • Capsules
    • Injectables
  5. 5OOS/OOT Handling
    • Root cause analysis
  6. 6Calibration & Maintenance
    • Instrument qualification basics
Final Project: Finished product analysis
Microbiology

Highly employable aseptic-handling track for injectables, vaccines and food industries.

6 modules
Core practical: Sterility testing
Modules
  1. 1Aseptic Techniques
    • Laminar airflow
    • Gowning procedures
  2. 2Sterility Testing
    • Media preparation
    • Incubation methods
  3. 3Environmental Monitoring
    • Air monitoring
    • Surface monitoring
    • Personnel monitoring
  4. 4Water Testing
    • Purified water
    • WFI analysis
  5. 5Microbial Limit Tests
    • Colony counting
    • Culture techniques
  6. 6Documentation
    • EM reports
    • Sterility reports
Final Project: Environmental monitoring study
Molecular Biology

PCR, sequencing and cloning workflows used in diagnostics, vaccines and precision medicine.

6 modules
Core practical: PCR
Modules
  1. 1Molecular Biology Basics
    • DNA/RNA concepts
  2. 2PCR Techniques
    • Conventional PCR
    • RT-PCR
  3. 3DNA/RNA Extraction
    • Isolation methods
    • Purification techniques
  4. 4Gel Electrophoresis
    • DNA separation
    • Visualization
  5. 5Sequencing Basics
    • Genomics introduction
  6. 6Cell Culture Basics
    • Media handling
    • Sterility
Final Project: PCR diagnostic workflow
Vaccine R&D / Biotech

Bioprocessing, immunology assays and fermentation inside India's leading vaccine makers.

5 modules
Core practical: ELISA
Modules
  1. 1Bioprocess Basics
    • Fermentation
    • Bioreactors
  2. 2Upstream Processing
    • Cell cultivation
    • Growth optimization
  3. 3Downstream Processing
    • Filtration
    • Purification
  4. 4Immunology
    • ELISA
    • Antigen-antibody reactions
  5. 5Vaccine Manufacturing
    • Viral vaccines
    • Recombinant vaccines
Final Project: Vaccine process overview
Validation

Equipment, process, cleaning and computer-system validation for USFDA-approved plants.

5 modules
Core practical: IQ/OQ/PQBest for: Injectable plants & USFDA-approved sites
Modules
  1. 1Equipment Qualification
    • IQ
    • OQ
    • PQ
  2. 2Process Validation
    • Validation protocols
    • Sampling plans
  3. 3Cleaning Validation
    • Swab sampling
    • Residue calculations
  4. 4CSV Basics
    • Software validation concepts
  5. 5Documentation
    • Validation reports
Final Project: Equipment qualification protocol
Regulatory Affairs

Dossier, CTD/eCTD and DMF/ANDA support for global submissions.

5 modules
Core practical: CTDBest for: M.Pharm, Pharm.D, regulatory-oriented students
Modules
  1. 1Regulatory Overview
    • USFDA
    • EMA
    • CDSCO
  2. 2Dossier Preparation
    • CTD
    • eCTD
  3. 3ANDA & DMF Basics
    • Filing structure
  4. 4Labeling & Artwork
    • Packaging compliance
  5. 5Submission Systems
    • Regulatory timelines
Final Project: CTD module preparation
Pharmacovigilance (PV)

Adverse event reporting, case processing and drug safety inside CROs and global pharma.

5 modules
Core practical: ADR processing
Modules
  1. 1Drug Safety Basics
    • ADR concepts
  2. 2Case Processing
    • ICSR handling
  3. 3MedDRA Coding
    • Terminology systems
  4. 4Signal Detection
    • Safety trends
  5. 5Global Safety Systems
    • Argus overview
Final Project: ADR case processing
Clinical Research

Trial coordination, ethics submissions and GCP-aligned site documentation.

5 modules
Core practical: CRF handling
Modules
  1. 1GCP Guidelines
    • Ethics
    • Trial regulations
  2. 2Clinical Trial Workflow
    • Phase I–IV studies
  3. 3Documentation
    • CRF
    • Informed consent
  4. 4Site Coordination
    • Monitoring basics
  5. 5Ethics Committee
    • Submission process
Final Project: Clinical trial documentation
Bioinformatics & Genomics

Fast-growing track combining NGS analysis, AI in biology and drug-discovery informatics.

5 modules
Core practical: BLAST
Modules
  1. 1Genomics Basics
    • DNA sequencing
  2. 2Bioinformatics Tools
    • BLAST
    • Sequence alignment
  3. 3NGS Basics
    • Data analysis
  4. 4Drug Discovery Informatics
    • AI in pharma
  5. 5Computational Biology
    • Database handling
Final Project: Sequence analysis project
Industrial Production / Manufacturing

Granulation to packaging — hands-on GMP manufacturing across solid and sterile dosage forms.

5 modules
Core practical: Granulation
Modules
  1. 1Production Workflow
    • Granulation
    • Compression
    • Coating
  2. 2Sterile Manufacturing
    • Injectable handling
  3. 3Packaging Operations
    • Blister packing
    • Labeling
  4. 4GMP Compliance
    • Manufacturing controls
  5. 5In-Process Checks
    • IPQA coordination
Final Project: Tablet manufacturing process
Food & Nutraceutical Analytical

Crossover track for pharma + food-tech students focused on FSSAI-aligned testing.

5 modules
Core practical: Nutraceutical analysis
Modules
  1. 1Food Testing Basics
    • Nutraceutical analysis
  2. 2Analytical Techniques
    • HPLC
    • Microbial analysis
  3. 3Food Microbiology
    • Contaminant testing
  4. 4Shelf-Life Studies
    • Stability concepts
  5. 5Regulatory Standards
    • FSSAI basics
Final Project: Nutraceutical product analysis
Common modules (all tracks)

Foundational modules every intern completes alongside their chosen specialization. Select a duration to preview only the modules included in that internship plan.

1 Month plan fee
₹4,999
+ 18% GST at checkout
13 of 72 modules
18% coverage
13 of 72 modules unlocked (18%)
Analytical R&D — Introduction to Analytical R&D
Pharma analytical workflow · GLP basics
Analytical R&D — Instrumentation
HPLC · UPLC · GC · UV Spectroscopy
Analytical R&D — Practical Training
Mobile phase preparation · Standard preparation · Sample analysis · Calibration
Analytical R&D — Method Development
Column selection · pH optimization · Resolution improvement
Analytical R&D — Method Validation
Accuracy · Precision · Specificity · Robustness
Analytical R&D — Stability Studies
Accelerated stability · Stability chamber handling
Analytical R&D — Documentation
Analytical reports · SOP preparation · Validation reports
Quality Assurance (QA) — GMP & Documentation
cGMP · GDP · Data integrity
Quality Assurance (QA) — SOP Systems
SOP drafting · Document control
Quality Assurance (QA) — Batch Documentation
BMR/BPR review · Line clearance
Quality Assurance (QA) — QA Systems
Deviations · CAPA · Change control
Quality Assurance (QA) — Audit Management
Internal audits · Regulatory inspections
Quality Assurance (QA) — Validation Overview
Process validation · Cleaning validation
Career outcomes
  • R&D associate roles
  • QA / regulatory tracks
  • Higher-studies admissions edge
  • Industry referrals