नेतृत्वाय शिक्षस्व (Netṛtvāya śikṣasva)
IILS offers a range of specialized certification courses designed exclusively for the healthcare and life sciences domains, these programs are led by industry-recognized, award-winning faculty with proven expertise, ensuring you master essential domain concepts with practical insights.
Professional Diploma in Clinical Research
ECR- 06 Months “24 Weeks” 120 Hrs “ 20 Hrs/M
Residential (Classroom) | Distance (Online)
Certificate
This program provides a strong foundation in clinical research, covering study design, protocol development, ethics and regulations, and ICH-GCP guidelines. It equips participants with practical knowledge of site operations, regulatory basics, and trial oversight to confidently step into the clinical research industry.
Professional Diploma in
Pharmacovigilance
EPV- 06 Months “24 Weeks” 120 Hrs “ 20 Hrs/M
Residential (Classroom) | Distance (Online)
Certificate
Designed for aspiring drug safety professionals, this certification focuses on the science of detecting, assessing, understanding, and preventing adverse effects. Students will explore global pharmacovigilance systems, case processing, signal detection, safety databases, and regulatory reporting under ICH and WHO guidelines.
Essentials of Clinical Data Management
ECDM- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program offers a comprehensive foundation in clinical data management, focusing on data collection, validation, processing, and database design. Participants will gain practical insights into CRF design and development, query management, and industry-standard tools, enabling them to ensure data integrity and contribute effectively to clinical trial success.
Essentials of Medical Writing
EMW- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program introduces participants to the core principles of medical writing, focusing on regulatory, scientific, and clinical documentation. It builds essential skills in structuring clinical study reports, informed consent forms, investigator brochures, and publications, ensuring clarity, accuracy, and compliance with global standards. Ideal for aspiring professionals in regulatory and scientific communication.
Essentials of Regulatory Affairs
ERA- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program offers a comprehensive introduction to global regulatory frameworks governing pharmaceuticals, biologics, and medical devices. It covers regulatory submissions, drug approval processes, lifecycle management, and key regulatory bodies like USFDA, EMA, and CDSCO. Participants gain the knowledge needed to navigate complex regulatory pathways and ensure product compliance in domestic and international markets.
Essentials of Quality Assurance
EQA- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program builds a solid foundation in quality assurance principles specific to the clinical research. It covers quality management systems, documentation practices, internal and external audits, CAPA, deviation handling, and risk-based quality control. Participants will be equipped to implement and monitor QA processes that ensure regulatory compliance and uphold industry standards.
Essentials of Trial Master File and eTMF
ETMF- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program offers in-depth knowledge of Trial Master File (TMF) and electronic TMF (eTMF) systems essential to clinical trial documentation. It covers TMF structure, essential documents, ICH-GCP compliance, document lifecycle management, audit readiness, and regulatory expectations. Participants will gain practical insights into maintaining a complete, accurate, and inspection-ready TMF/eTMF environment.
Essentials of Medical
Monitoring
EMM- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This course provides a practical introduction to medical monitoring in clinical trials. It covers safety data review, protocol adherence, medical oversight responsibilities, SAE management, and collaboration with clinical teams. Participants will develop the skills needed to ensure patient safety, data integrity, and regulatory compliance throughout the trial process.
Essentials of Audit and Inspection
EAI- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program offers a comprehensive understanding of audits and inspections in clinical research and pharmaceutical settings. It covers audit planning, types of audits, inspection readiness, regulatory requirements, and CAPA implementation. Participants will gain the skills to ensure organizational compliance and confidently manage audit and inspection processes.
GxP standards
Good Clinical Practice
GCP- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program provides in-depth knowledge of ICH-GCP guidelines, ethical conduct, subject protection, and regulatory compliance in clinical trials. It emphasizes investigator responsibilities, sponsor obligations, documentation practices, and quality standards, preparing participants to uphold the highest levels of integrity and compliance in clinical research.
Good Laboratory Practice
GLP- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This course offers a comprehensive understanding of Good Laboratory Practice principles essential in non-clinical research and laboratory environments. It covers study conduct, SOPs, data integrity, equipment calibration, documentation, and audit readiness—ensuring participants meet quality and regulatory expectations in preclinical and analytical settings.
Good Manufacturing Practice
GMP- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This course provides a structured overview of Good Manufacturing Practice (GMP) guidelines critical to pharmaceutical and biotech production. It covers facility requirements, process validation, documentation practices, deviation and change control, quality systems, and regulatory compliance—preparing participants to ensure product safety, efficacy, and consistency across manufacturing operations.
Computer System Validation
GPV- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program introduces the principles of Good Pharmacovigilance Practice, focusing on adverse event reporting, signal detection, risk management plans, periodic safety update reports (PSURs), and regulatory requirements. Participants will gain a deep understanding of global pharmacovigilance systems, ensuring compliance and patient safety throughout the drug lifecycle.
Good Documentation Practice
GDP- 03 Months “12 Weeks” 120 Hrs “ 20 Hrs/M
Certificate
This course provides a detailed understanding of documentation standards critical to regulatory compliance in healthcare and life sciences. It covers ALCOA+ principles, controlled documents, data integrity, audit trails, SOP writing, and documentation audits. Participants will develop the skills to create, manage, and maintain accurate, reliable, and compliant records across regulated environments.
Good Pharmacovigilance Practice
CSV- 03 Months “12 Weeks” 60 Hrs “ 20 Hrs/M
Certificate
This program introduces participants to the principles and regulatory requirements of computer system validation in the healthcare and pharmaceutical industries. It covers system lifecycle, risk-based validation, 21 CFR Part 11 compliance, data integrity, and documentation practices. Learners gain hands-on insights into validating software and systems to ensure they meet GxP compliance standards.