Advanced Training Program on Drug Development and Analysis

The Advanced Training Program on Drug Development and Analysis is a comprehensive 15-day summer school designed to provide in-depth knowledge and practical exposure to the key stages of drug discovery, formulation, and evaluation. Aligned with the vision of National Education Policy 2020, the program emphasizes experiential learning, skill development, multidisciplinary education, and industry integration to enhance the employability and competence of pharmacy students. The curriculum covers essential aspects of drug development, including preformulation studies, formulation of solid and liquid dosage forms, and evaluation parameters for quality assurance. Participants will gain practical experience with advanced analytical tools such as UV-Visible spectroscopy and High-Performance Liquid Chromatography (HPLC), along with an understanding of calibration, validation, and data interpretation. In addition, the program introduces regulatory requirements, including ICH guidelines and quality control standards followed in pharmaceutical industries. Sessions on research methodology, scientific writing, and data analysis are incorporated to strengthen research aptitude in accordance with outcome-based education principles advocated by NEP 2020. Through a combination of expert lectures, hands-on laboratory sessions, case studies, and mini-projects, the program fosters critical thinking, innovation, and problem-solving skills. By the end of the training, participants will be well-prepared to pursue careers in pharmaceutical industries, research and development, and higher education, contributing effectively to the evolving healthcare and pharmaceutical sector.

Duration

2 Weeks

Skill Level

Moderate

Starts From:

27/07/2026

Category

Science And Technology

Overview

The Advanced Training Program on Drug Development and Analysis is a comprehensive 15-day summer school designed to provide in-depth knowledge and practical exposure to the key stages of drug discovery, formulation, and evaluation. Aligned with the vision of National Education Policy 2020, the program emphasizes experiential learning, skill development, multidisciplinary education, and industry integration to enhance the employability and competence of pharmacy students.
The curriculum covers essential aspects of drug development, including preformulation studies, formulation of solid and liquid dosage forms, and evaluation parameters for quality assurance. Participants will gain practical experience with advanced analytical tools such as UV-Visible spectroscopy and High-Performance Liquid Chromatography (HPLC), along with an understanding of calibration, validation, and data interpretation.
In addition, the program introduces regulatory requirements, including ICH guidelines and quality control standards followed in pharmaceutical industries. Sessions on research methodology, scientific writing, and data analysis are incorporated to strengthen research aptitude in accordance with outcome-based education principles advocated by NEP 2020.

Through a combination of expert lectures, hands-on laboratory sessions, case studies, and mini-projects, the program fosters critical thinking, innovation, and problem-solving skills. By the end of the training, participants will be well-prepared to pursue careers in pharmaceutical industries, research and development, and higher education, contributing effectively to the evolving healthcare and pharmaceutical sector.


Our Trainers

Ms. Rekha Birle

Assistant Professor

Institute of pahrmacy

Sage University, Indore

Dr. Hemant Khambete

Professor,Head of Department,

Faculty of Pharmacy

Medicaps University, Indore

Ms. shivanee Patidar

Assistant Professor,

Institute of Pharmacy

Sage university

Mr. Ankit Anchliya

Assistant Professor

Dr. Suresh Kumar Paswan

Associate Professor at Shri G. S. Institute of Technology & Science, Indore

Modules

1. Hands-on Practical Training: Extensive laboratory exposure in pharmaceutical formulation and evaluation techniques 2. Comprehensive Drug Development Modules: Coverage of preformulation, tablet, capsule, and liquid dosage forms 3. Advanced Analytical Techniques: Practical training on UV-Visible Spectroscopy, HPLC, and instrument calibration. 4. Expert Sessions: Interactive lectures by academicians and industry professionals 5. Industrial Exposure: Industrial visit or virtual tour to understand pharmaceutical manufacturing 6.Certification: Certificates of participation and excellence for successful candidates


Outcomes

CO No. Course Outcome Statement Bloom’s Level
CO1 Explain the stages involved in drug discovery, development, and evaluation K2 – Understand
CO2 Describe principles and applications of preformulation studies K2 – Understand
CO3 Demonstrate formulation techniques for solid and liquid dosage forms K3 – Apply
CO4 Apply evaluation and quality control parameters for dosage forms K3 – Apply
CO5 Analyze data obtained from UV-Visible Spectroscopy and HPLC K4 – Analyze
CO6 Apply calibration, validation, and ICH regulatory guidelines K3 – Apply
CO7 Evaluate research data and present findings using scientific writing K5 – Evaluate
CO8 Develop innovative solutions and problem-solving skills in pharmaceutical sciences K6 – Create

FAQs

1. What is the duration of the program?

The program is a 15-day intensive summer training designed to provide both theoretical knowledge and practical exposure.


2. Who can apply for this program?

This program is suitable for:

  • B.Pharm / M.Pharm students
  • Pharmacy diploma students
  • Recent graduates interested in pharmaceutical sciences

3. What topics are covered in the program?

The program includes:

  • Drug discovery and development
  • Preformulation studies
  • Solid and liquid dosage form formulation
  • Analytical techniques (UV-Visible, HPLC)
  • Calibration and validation
  • ICH regulatory guidelines
  • Research methodology and scientific writing

4. Will there be practical/laboratory training?

Yes, the program includes hands-on laboratory sessions on formulation and analytical techniques.


5. What analytical instruments will participants learn?

Participants will gain experience with:

  • UV-Visible Spectrophotometer
  • High-Performance Liquid Chromatography (HPLC)

6. Is the program aligned with NEP 2020?

Yes, the program follows NEP 2020 guidelines, focusing on experiential learning, skill development, and industry readiness.


7. Will participants receive a certificate?

Yes, a certificate of completion will be awarded after successful participation.


8. How will this program benefit my career?

The program helps in:

  • Building industry-relevant skills
  • Enhancing practical knowledge
  • Improving employability in pharma industries and R&D

9. Are there any assessments or projects?

Yes, participants will engage in:

  • Mini-projects
  • Case studies
  • Practical evaluations

10. Do I need prior laboratory experience?

No, basic knowledge of pharmacy is sufficient. All necessary training will be provided.


11. What is the mode of teaching?

The program includes:

  • Expert lectures
  • Hands-on training
  • Case studies and interactive sessions

12. How can I register for the program?

Registration details will be provided through the official brochure/website of the institute.


Contact

Name: Dr Kushboo Arora

Mobile No: 9926018700


Course Image

This Premium course is included in plans

1000/-

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