Prospectus

The Institute of Good Manufacturing Practices India, an autonomous Institute recognised by Ministry of Commerce & Industry, accredited Vocational Institution of Ministry of Education, Government of India and approved by Food Safety and Standards Authority of India (FSSAI), presents a unique, friendly and interactive platform to get rid of all your GMP compliance related issues. GMP—an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing and sustainability services—in itself is the most dynamic part which witnesses frequent changes in terms of new rules being added and old ones being renewed. Thus, keeping oneself updated with current GMPs is essential to remain aligned with evolving industry requirement and standards.

Our team comprises knowledgeable professionals from diverse sectors such as Pharma, Healthcare, Food, Nutraceutical, and Nutrition industries, pooling together their expertise, know-how, and experiences to create this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as a stronger and better education and training platform provider for professionals and students in the areas of GMP, Quality Assurance and Control, Pharma, Food & Nutrition, Environment and Healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR, Good Laboratory Practice and Product Management. Keeping pace with the digital era, IGMPI has also expanded into the domains of Geoinformatics, Remote Sensing, Cybersecurity, Information Security, and Network Security, preparing learners to address the growing need for secure and resilient information systems as well as advanced geospatial solutions.

Our board of governors and specialists have collated their acumen and are offering state-of-the-art courses which include GMP training, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR, Environment Social Governance (ESG), Good Laboratory Practice, Information Security Compliance and Remote Sensing. These are delivered in the form of formal classroom studies, online/interactive programmes, online seminars, and onsite training programmes, along with insights into global industry practices. In short, a round-the-clock service is provided for any information in these areas required by anybody from around the country and abroad.

Based on high standards of quality, the training programmes in Pharma, Healthcare and Food GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management, Public Health, Hospital Management, Clinical Research, Pharmacovigilance, Medical Writing, Medical Coding, Nanotechnology, Drug Design and Discovery, Food QA&QC have been approved by the Quality Council of India, which is an autonomous body and an accreditation authority for education & vocational training providers under the Ministry of Commerce & Industry, Government of India. IGMPI is duly licensed and certified by Bureau of Indian Standards (BIS) under Bureau of Indian Standards (Conformity Assessment) Regulations 2018.

The Post Graduate and Executive Diploma programmes of IGMPI in Good Manufacturing Practices, Regulatory Affairs, Intellectual Property Rights, Quality Assurance and Quality Control, Public Health, Nanotechnology, Hospital Management, Product Management, Sales and Marketing Management, Clinical Research, Medical Writing, Drug Discovery and Development, Pharmacovigilance, Medical Coding have been duly assessed and approved by Quality Council of India, Government of India based on fulfillment of QCI's following criteria:

    1. Course Content
    2. Course Design
    3. Course Material
    4. Instructors
    5. Class size & Attendance
    6. Facilities
    7. Evaluation of Students
    8. Written Examination
    9. Certificate

IGMPI is also approved by Food Safety and Standards Authority of India (FSSAI) (FSSAI ID: TPINS18). IGMPI® is licensed by Department of Food Safety & Drug Administration under the Drugs and Cosmetics Act, 1940 and registered under Food Safety and Standards Act 2006.

IGMPI is also approved by Sector Skills Council under National Skill Development Corporation (NSDC) setup by Ministry of Skill Development & Entrepreneurship, Govt of India (TC ID:TC342267).

IGMPI has been conferred with the prestigious "BUREAU OF INDIAN STANDARDS (BIS) AWARD OF HONOUR 2023". QUALITY COUNCIL OF INDIA (QCI) has also conferred IGMPI with D.L. SHAH NATIONAL QUALITY AWARD, Certificate of Merit & ASSOCHAM has conferred IGMPI with the Services Excellence Award based on excellence of its services to the students and training participants.

Bureau of Indian Standards (BIS) is a member of International Organization for Standardization (ISO) and through the Indian National Committee (INC) which is a member of International Electrotechnical Commission (IEC). BIS is also a member of regional standards bodies like Pacific Area Standards Congress (PASC) and South Asian Regional Standards Organization (SARSO). India started taking part in IEC from 1911 and subsequently the then Indian Standards Institution (now BIS) took over the responsibility of Indian National Committee of IEC(INC-IEC) in 1949. Since then the INC-IEC is actively participating in the activities of the IEC both at the policy level and technical work and carrying out the responsibilities as member body of IEC Council. India is a member in Standards Management Board (SMB) of IEC since 2015.BIS has also signed Bilateral Cooperation Agreements (BCA)/Mutual Recognition Agreements (MRA) with the National Standards Bodies of several countries like Afghanistan, Bangladesh, Belarus, Egypt, European Union , Germany, Ghana, Greece, Indonesia, Iran, Japan, Jordon, Kenya, Kyrgyzstan, Mali, Mauritius, Nigeria, Russia, Saudi Arabia , Slovakia, Slovenia, Suriname, USA, UAE, Uzbekistan, Viet Nam, Bhutan, Brazil, Israel, Nepal, Pakistan and Sri Lanka.

National Accreditation Board for Certification Bodies (NABCB), Quality Council of India is a member of International Accreditation Forum (IAF) & Pacific Accreditation Cooperation (PAC) as well as signatory to its MLAs for Quality Management Systems, Environmental Management Systems and Product Certification. NABCB is also a Full Member of International Laboratory Accreditation Cooperation (ILAC) & Asia Pacific Laboratory Accreditation Cooperation (APLAC) as well as signatory to its MRAs for Inspection.

Course description

Computational Pharmaceutics is an emerging interdisciplinary field that integrates pharmaceutical sciences, mathematical modelling, computational simulations, data analytics, and artificial intelligence to improve the development, optimisation, and performance of pharmaceutical products. It involves the application of computational approaches to understand drug properties, predict formulation behaviour, model drug release and absorption, and evaluate drug delivery systems. The programme focuses on the application of computational methods across preformulation, pharmaceutical formulation development, biopharmaceutics, pharmacokinetics, physiologically based pharmacokinetic (PBPK) modelling, and pharmaceutical process optimisation. It introduces learners to data-driven approaches for predicting critical quality attributes, optimising formulation variables, understanding drug-excipient interactions, and assessing the influence of physiological and formulation parameters on drug performance.

Designed in response to the growing adoption of digital technologies and model-informed approaches in the pharmaceutical industry, it is suitable for pharmacy graduates, pharmaceutical scientists, researchers, and professionals seeking to strengthen their expertise in formulation development, drug delivery, pharmacokinetics, and computational pharmaceutical research. The programme combines theoretical learning with software-based practical exercises, industry-relevant case studies, and a capstone project. It serves as a refresher and upskilling opportunity for professionals already working in the pharmaceutical sector, while also providing an introduction to computational methods for graduates aspiring to enter pharmaceutical research, formulation development, biopharmaceutics, and related scientific roles. 

Target audience

The programme is suitable for:

• Students and graduates in pharmacy, pharmaceutical sciences, medicinal chemistry, chemistry, biotechnology, biochemistry, bioinformatics and related life sciences.
• Postgraduate students and research scholars seeking to apply computational methods to drug discovery research.
• Scientists and research associates involved in compound screening, lead optimisation, molecular modelling and drug repurposing.
• Academicians and teaching professionals seeking to strengthen their knowledge of computational drug design and its practical applications.

A foundational understanding of chemistry and biology is desirable. Introductory computational concepts will be addressed to support participants from diverse academic backgrounds. 

Programme structure

Module 1. Fundamentals of Computational Pharmaceutics

• Introduction, scope and evolution of computational pharmaceutics
• Traditional versus computational approaches to pharmaceutical development
• Applications in preformulation, formulation development and drug delivery 

Module 2. Physicochemical Principles and Preformulation Modelling

• Solubility, pKa, partition coefficient and ionisation
• Dissolution, diffusion and drug permeability
• Solid-state properties, polymorphism and amorphous systems
• Drug-excipient compatibility and material properties
• Computational prediction of solubility and physicochemical behaviour

Module 3. Mathematical Modelling, Statistics and Data Analysis

• Essential mathematics for pharmaceutical modelling
• Descriptive statistics, probability and hypothesis testing
• Regression, correlation and model fitting
• Error analysis, uncertainty and sensitivity analysis
• Introduction to Python, spreads sheets and scientific data visualisation 

Module 4. Computational Formulation Development and Optimisation

• Preformulation and formulation design
• Design of Experiments (DoE) and Quality by Design (QbD)
• Factorial designs, response surface methodology and optimisation
• Predictive models for tablet, capsule and liquid formulations

Module 5. Drug Release, Dissolution and Biopharmaceutic Modelling

• Drug dissolution and release mechanisms
• Zero-order, first-order, Higuchi and Korsmeyer-Peppas models
• In vitro dissolution data analysis
• IVIVC and IVIVR concepts and applications 

Module 6. Fundamentals of Pharmacokinetics and PK Data Analysis

• ADME and concentration-time relationships
• Linearity and non-linearity in pharmacokinetics
• Compartmental and non-compartmental analysis
• AUC, Cmax, Tmax, clearance, half-life and volume of distribution 

Module 7. Physiologically Based Pharmacokinetic (PBPK) Modelling

• Classical pharmacokinetic models versus PBPK models
• Model structure, Model development, assumptions and physiological parameters
• Drug-specific versus system-related input parameters
• Organ compartments, blood flow and tissue distribution

Module 8. Population Pharmacokinetics and Pharmacokinetic-Pharmacodynamic Modelling

• Population PK concepts and mixed-effects modelling
• Inter-individual and intra-individual variability
• Covariate analysis and special populations
• PK-PD relationships and exposure-response modelling
• Applications in clinical development and generic products

Module 9. Molecular Modelling and Computational Drug-Excipient Interactions

• Molecular structures, energy minimisation, interaction analysis
• Molecular mechanics and molecular dynamics fundamentals
• Molecular-level interpretation of compatibility and stability 

Module 10. Biopharmaceutics, ADME Prediction and Bioavailability

• Biopharmaceutics Classification System (BCS)
• Solubility, permeability and bioavailability relationships
• In silico ADME prediction and its limitations
• Food effects, drug interactions and absorption variability
• Linking formulation characteristics to systemic exposure 

Module 11. Process Modelling, Digital Twins and Pharmaceutical Manufacturing

• Modelling of blending, granulation, drying and tableting
• Process parameters and critical quality attributes
• Process analytical technology and data integration
• Digital twins and process simulation concepts
• Scale-up, technology transfer and manufacturing optimisation 

Module 12. Model Validation, Regulatory Science and Data Integrity

• Model qualification, verification and validation
• Good Modelling Practice principles and documentation
• ICH Q8, Q9 and Q10 concepts relevant to pharmaceutical development
• Data integrity, reproducibility, version control and audit trails 

Eligibility

Graduates in any discipline are eligible for our Post Graduate Diploma, Executive Diploma and Professional Certifications Programmes. 10+2 pass-outs are eligible for our Under Graduate Diploma and Diploma holders of two to three years course duration are also eligible for the PG Diploma.

Programme Duration

The minimum duration to complete the PG diploma programme is 12 months and maximum is 24 months. The minimum duration to complete the executive diploma programme is 6 months and maximum is 12 months.

Programme Mode

Registrations are currently open for regular and Part-time (Online Live Classes) both modes.

Programme Deliverables

The accompanying training is appropriately aligned with the current Industry’s expectations.

• Interactive or online live sessions on all key areas of the programme giving all flexibility to the participants.
• All the efforts are made by IGMPI faculty members to make the entire programme modules easily understandable.
• Assessment and evaluation for all the programme modules in order to enhance the levels of competencies and skills of the participants leading towards the objective of application in the job.
• At the end of each programme modules, the trainers shall obtain feedback from the participants using specially designed questionnaires.
• All learning and training delivery initiatives shall be conducted in English. 

Examination & Certification

All the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma/Executive Diploma in Computational Pharmaceutics by IGMPI. For all the above-mentioned modules, Part-time (Online Live Classes) or face-to-face classes (Regular mode), elaborate programme material, self-assessment assignments would be provided by the Institute. Details get updated on the webpage as well. 

Discipline in Classes and Examination

Every student is required to observe a disciplined behaviour during her/his classes, assessments & examinations and to follow instructions from the Professors. Any act of indiscipline may result into discredit & it will be mentioned in her/his academic report.

Placement Assistance & Corporate Relations

For the Post Graduate Diploma, Undergraduate Diploma, Executive Diploma and Professional Certification Programmes, we will provideplacement assistance after the completion of the programme. The Institute has partnered with many organizations for providing placement assistance to its students. The robust placement cell comprises senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. The efforts of our placement cell also include helping with professional resume writing, interview skills & conducting mock interviews etc.

In recent months the Institute has witnessed more and more participation from professionals working with global healthcare like , Jhpiego, SELCO Foundation, TATA Foundation, Samarthan NGO, PSI, UNICEF, WHO, HCL Foundation, IPE Global, Optum, PATH, AIIMS, Action against Hunger, Ekta Shakti Foundation, Seva Foundation, India HIV-AIDS Alliance, HLFPPT, Deepak Foundation, Novartis, LalPath Labs Ltd., Fortis Healthcare Ltd., HealthCare Global Enterprises Ltd., Indraprastha Medical Corporation Ltd., Narayana Hrudayalaya Ltd., Piramal Enterprises Ltd., Wockhardt Ltd., Cactus Communications, Public Health Foundations of India, Cytel, Religare Health Insurance Company Ltd., Deloitte, DuPont Sustainable Solutions, Bain & Company, Alvarez & Marsal, McKinsey & Company, etc. The IGMPI’s Corporate Resource Division actively recommends our students and training participants for various job requirements and specialized roles to Human Resource, Talent Acquisition as well as the heads of various departments in Pharmaceutical, Healthcare industries on regular basis.

Future Prospects

Knowledge gained through this programme can support participants in exploring research and professional opportunities in pharmaceutical companies, biotechnology organisations, contract research organisations (CROs), academic institutions and pharmaceutical technology start-ups working in computational pharmaceutics and data-driven research. Depending on their academic qualifications and practical experience, participants may pursue roles such as Computational Pharmaceutics Research Associate, Formulation Development Research Associate, Pharmacokinetic Modelling Associate, PBPK Modelling Research Associate, Pharmaceutical Data Analyst, AI/ML Research Associate in Pharmaceutical Sciences, or Drug Delivery Research Associate. The programme also provides a foundation for postgraduate research, doctoral studies and further specialisation in computational pharmaceutics, pharmaceutical modelling, biopharmaceutics, pharmacokinetics, formulation optimisation and artificial intelligence in pharmaceutical development. Through practical exercises and the capstone project, participants can develop skills in computational analysis, model interpretation, formulation prediction and evidence-based decision-making. Career progression will depend on relevant academic qualifications, practical project experience, proficiency in computational tools and programming, and continued professional development.