Rapture Biotech

+91 991-018-1655, +91 836-803-9229
rapturebio@gmail.com
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Program Overview

Rapture Biotech’s pharmaceutical training program is a game-changing opportunity for future pharmaceutical professionals, offered by India’s No.1 Biotech Training Company. This program provides hands-on, cutting-edge training in pharmaceutical sciences, including drug development, pharmacology, pharmaceutical analysis, formulation science, regulatory affairs, and quality control.

Participants will gain practical experience in advanced lab techniques such as drug synthesis, stability testing, and pharmacokinetic studies. Under expert supervision, you’ll develop critical skills and in-depth knowledge that will give you a competitive edge in the pharmaceutical industry.

Offered across major cities like Noida, Chandigarh, Dehradun, Gwalior, Jaipur, Gujarat, Mumbai, Chennai, Hyderabad, and Jammu, this program is designed to equip the next generation of pharmaceutical innovators with the expertise to thrive in the industry.

ADVANCED TECHNICAL MODULES (JOB ORIENTED)

Module 1- Phytochemistry and Pharmacognosy
  1. Introduction and application of Phytochemistry and Pharmacognosy and Herbal Standardization.
  1. GACP (Good Agricultural and Collection Practices).
  2. ALCOA / ALCOA+ principles in laboratory records.
  3. Calculation (Percentage, Molarity and Normality) and micropipette handling (Reverse and Forward pipetting).
  4. Introduction to Quality Assurance (QA) and Quality Control (QC).
  5. Standard Operating Procedure (SOP) of module related instruments.
  6. Safety in handling phytochemicals & solvents.
  7. Determination of moisture content of crude drugs.
  8. Standard procedure of herbal extract preparation (Maceration/Decoction).
  9. Extract yield calculation (Water and Alcohol).
  10. Determination of alcohol-soluble extractive value of plant material.
  11. Qualitative phytochemical determination of crude extract.
  12. Quantitative estimation of Phytochemical (Phenolic/ Tannin/ Flavonoid) through UV visible spectrophotometer
  13. Standard Curve preparation and Data Interpretation.
  14. Evaluation of Antioxidant Activity of Herbal extract via Thin Layer Chromatography (TLC).
  15. Separation and identification of curcuminoids from curcumin via TLC method.
  16. Separation of active constituents of clove by thin layer chromatography (TLC).
  17. Basic concept of Purification of herbal extract by Column chromatography.
  18. Introduction and Industrial Application of HPLC (T).
Module 2- Pharmaceutical Microbiology
  1. Introduction, Scope and importance of Pharmaceutical Microbiology.
  1. Maintenance of laboratory area and related monitoring records as applicable.
  2. General and safety rules for working in the Laboratory and Rules and precautions for the microbiological laboratory.
  3. Micropipette handling (forward and reverse pipetting) and Overview on Microscope.
  4. Sterilization and disinfection.
  5. Sterilization of glass wares and Bacteriological analysis of water.
  6. Preparation & sterilization of media and Subculturing of bacteria.
  7. Standard Plate Count (SPC) / CFU calculation.
  8. To identify the given bacterial culture by gram staining method.
  9. Cultivation of microbes in a nutrient broth and nutrient agar medium by spread plate and streak plate techniques.
  10. Isolation of pure culture by pour plate method.
  11. To study the characterization of microbes through biochemical reactions.
  12. To study oligodynamic action of metal on microbes.
  13. Motility test of bacterial culture.
  14. Microbiological assay of antibiotics of cup plate method.
  15. Investigation of microbial contamination in finished pharma products.
  16. To demonstrate bactericidal effect of UV light.
  17. Biosafety and waste disposal.
  18. Preparation and maintenance of microbial records (T).
Module 3- Quality Control Analysis of Syrups and Elixirs
  1. Introduction to pharmaceutical QC analysis and role of QC in liquid oral dosage forms.
  2. Good Laboratory Practices (GLP), GMP awareness and laboratory safety rules.
  3. SOP, STP and QC documentation practices.
  4. ALCOA / ALCOA+ and data integrity in pharmaceutical laboratories.
  5. Basic instrument handling and Basic concept of Percentage.
  6. Basic concept of molarity and normality.
  1. Microbiological quality analysis of Syrups/Elixirs.
  2. Determination of pH and viscosity.
  3. Moisture analysis and Weight/ml (Density) analysis of different Syrup/ Elixirs samples.
  4. UV-VIS Spectrophotometric analysis for added color.
  5. Physical stability test of liquid orals.
  6. Determination of alcohol concentration (only for elixirs) Via Spectrophotometer.
  7. Sucrose concentration/Assay of active ingredient through UV-VIS spectrophotometer.
  8. Accelerated stability studies in different syrups.
  9. Titratable acidity of different syrups.
  10. Analysis of natural sweetners in flavoured syrups.
  11. Refractometric analysis and Brix determination.
  12. Solubility test and Identification of active ingredients.
  13. Regulatory requirements: IP, USP, BP, Schedule M, WHO GMP and ICH awareness (T).
Module 4- Pharmaceutical Quality Control Analysis of Tablets and Capsules
  1. Introduction to pharmaceutical industry, dosage forms, and role of QC & QA.
  2. Good Laboratory Practices (GLP) and laboratory safety in pharmaceutical industries.
  3. SOP, documentation practices, and instrument handling basics.
  4. ALCOA / ALCOA+ and data integrity in pharmaceutical laboratories.
  5. Introduction to pharmacopoeial standards (IP/USP/BP).
  6. Basic laboratory calculations: percentage, molarity, normality, and dilution.
  7. Basics of spectrophotometry and analytical principles used in pharmaceutical QC.
  8. Introduction to in-process quality control (IPQC) and finished product testing.
  9. Micropipette handling (forward and reverse pipetting techniques).
  10. Loss on drying (LOD) analysis for moisture and volatile matter determination.
  11. Thickness and diameter measurement of tablets/capsules.
  12. Tablet hardness test for mechanical strength evaluation.
  13. Determination of disintegration time of tablets/capsules.
  14. Content uniformity testing of tablets/capsules by spectrophotometer.
  15. Qualitative identification of Acetaminophen.
  16. Percentage purity / assay of Acetaminophen by spectrophotometric method.
  17. Dissolution profiling of capsules.
  18. Microbiological quality / antimicrobial evaluation of tablets/capsules.
  19. Moisture content determination by Karl Fischer titrimeter.
  20. Capsule deformation and shell integrity evaluation.
Module 5: Pharmaceutical Chemistry – Quality Control, Quality Assurance and Analytical Techniques
  1. Introduction to Pharmaceutical Quality Control and Career Opportunities.
  2. Good Laboratory Practices (GLP) and Laboratory Safety in Pharmaceuticals.
  3. Demonstration of Laboratory Instruments and Clean Room Concept
  4. 5P principle in pharma industry.
  5. Micropipette Handling: Forward and Reverse Pipetting Techniques.
  6. Determination of Tablet Hardness Using Tablet Hardness Tester.
  7. Basic Principles of Limit Tests in Pharmaceutical Analysis.
  8. Limit Tests for Heavy Metals (Lead), Sulphate, and Chloride.
  9. Qualitative Analysis of Iodoform, Oxalic Acid, and Ester.
  10. Introduction to Minimum Inhibitory Concentration (MIC).
  11. Determination of MIC of Antibiotics Against Pathogenic Bacteria.
  12. Qualitative Assay of Acetaminophen.
  13. Percentage Purity Analysis of Paracetamol from Different Brands Using UV-Visible Spectrophotometry.
  14. Biochemical Assay of Ibuprofen.
  15. Percentage Purity Analysis of Ethanol in Dettol Using Spectrophotometric Method.
  16. Purity Assessment of Aspirin from Different Tablet Formulations.
  17. Basic Concept of Moisture Analysis in Tablets Using Karl Fischer Titration.
  18. Analysis of Different Salts Using Flame Test.
  19. Overview and Principle of Flame Photometry (T).
Module 6: Quality Analysis and Quality Control of Active Pharmaceutical Ingredients (APIs)
  1. Introduction to Active Pharmaceutical Ingredients (APIs) and Quality Analysis.
  2. Good Laboratory Practices (GLP) in Pharmaceutical Analysis.
  3. Handling and Operation of Basic Laboratory Instruments.
  4. Preparation and Standardization of Laboratory Solutions.
  5. Basic Pharmaceutical Calculations.
  6. Micropipette Handling and Qualitative Identification of Acetaminophen.
  7. Identification of Pantoprazole Sodium by Chemical Methods.
  8. Qualitative Detection of Aspirin in Different Tablet Formulations.
  9. Preliminary Quality Evaluation of Diclofenac Sodium.
  10. Limit Test for Chloride in Pharmaceutical Ingredients.
  11. Limit Test for Sulphate in Pharmaceutical Samples.
  12. Limit Test for Iron in Active Pharmaceutical Ingredients.
  13. Limit Test for Heavy Metals in Pharmaceutical Substances.
  14. Identification of Hydrochloride Salts by Silver Nitrate Test.
  15. Study of Pharmaceutical Ingredients Susceptible to Microbial Contamination.
  16. Basic Antimicrobial Evaluation of Antibiotics Using MIC and MBC Methods.
  17. Chromatographic Analysis of Acetaminophen.
  18. Documentation, Recording, and Reporting of Analytical Results.
  19. Sources of Errors in Pharmaceutical Analysis and Their Minimization (T).
Module 7- Biopharmaceuticals and Bacterial Vaccine Development
  1. Introduction to Biopharmaceuticals and types of Biopharmaceutical Products.
  2. Introduction to Vaccines and Immunization.
  3. Types of Vaccines.
  4. Regulatory Agencies and Government Guidelines.
  5. Good Laboratory and Manufacturing Practices.
  6. Biologics License Application (BLA) and Regulatory Documentation.
  7. Overview of Bacterial Vaccine Development.
  8. Basic Laboratory Calculations.
  9. Isolation and Screening of Bacterial Strains (Escherichia coli on Sorbitol MacConkey Agar).
  10. Confirmation and Identification of Bacterial Strains.
  11. Culture Maintenance Techniques.
  12. Optimization of Microbial Growth.
  13. Seed Culture Preparation for Fermentation.
  14. Fermentation and Scale-Up Techniques.
  15. Demonstration of Bioreactor/Fermentor Operation.
  16. Culture Proliferation and Harvesting of Bacterial Cells.
  17. Antigen Production, Identification, and Inactivation (Ouchterlony double diffusion).
  18. Downstream Processing, Vaccine Formulation, and Quality Control (T).
Module 8: Next-Gen Cancer Vaccine Designing using AI & Bioinformatics
  1. Introduction to Cancer & AI in Healthcare – Basics of cancer and how AI is used in modern biology.
  2. Finding Target Proteins (Easy Method) – Using databases like NCBI/UniProt with guided steps.
  3. Smart Antigen Selection – Using AI-based tools to quickly identify important proteins.
  4. Easy Epitope Prediction – Using tools like IEDB with simple selection methods.
  5. Safety Check using AI Tools – Allergenicity and toxicity prediction using AllerTOP and ToxinPred.
  6. AI-Based Epitope Selection – Selecting best epitopes using simple rules (high score, safe, effective).
  7. Vaccine Design Made Easy – Combining epitopes using simple logic and linkers.
  8. Structure Prediction using AI – Introduction to AlphaFold and basic visualization.

(Available at– NOIDA, Gujarat, Mumbai, Chandigarh, Chennai, Hyderabad, Jaipur, Dehradun, Gwalior)

(T) Stands for theory

Pharma Advanced Technical Modules Fees

Registration Fee- 1000/-(Excludes Program Fee)
Duration Indian candidates International Candidate ELIGIBILITY
7 day ₹ 4,000 (Any one module) 100$ All Life science students, Graduates or post graduates, pursuing or passed out students can apply. Ph.D. scholars, College faculties, working professionals can also apply
15 day ₹ 5,000 (Any two module) 120$
21 day ₹ 7,500 (Any three module) 180$
30 day ₹ 10,000 (Any four module) 240$
45 day ₹ 15,000 (Any six module) 350$
2 Months ₹ 17,000 400$
3 Months ₹ 21,000 520$
Additional Training
HPLC ₹ 4,000
Soft skills Training ₹ 3,000

Batch Timings: 10:00 A.M- 2:30 P.M (Morning) & 2:00 P.M - 6:30 P.M (Evening). Batch starts from every Monday, enrolled students can join from any Monday.

ELIGIBILITY

  • All Life science students, Graduates or post graduates, pursuing or passed out students can apply.
  • PhD scholars, College faculties, working professionals can also apply

Note: GST additional as per applicable.

Trainee may opt any above module on 1 week 1 module basis, as per interest.

*Centre has all the right to change modules, as per availability. 

Nearby Accommodation/Pgs & Hostel facility in 6,000/- per month (cost varies)

How to Apply

1️⃣ Fill the “Apply Online” Form.

2️⃣ Pay the Registration Fees – ₹1000 via UPI on 9910181655.
3️⃣ Send the screenshot of your payment via Whatsapp on 9910181655 with Name & Center.

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