Computer System Validation (CSV) Fundamentals
This online certification course explains the essential practices of Computer System Validation (CSV) and the GAMP 5 framework. It will […]
Certification Course
Fundamentals of EU GMP Annex 1
This is an essential online course designed to provide you with a comprehensive and practical understanding of the global standard
Management of Regulatory Audits and Inspections
This essential online course provides a comprehensive foundation you need to successfully navigate pharmaceutical audits and inspections. It equips you
Practical Understanding of Data Integrity in Pharma Industry
Data integrity is the foundation of a reliable Quality Management System (QMS) and is essential for safeguarding patient health and
EU GMP Annex 11: A Complete Overview of Computerised Systems
This essential online course provides a comprehensive foundation in EU GMP Annex 11, the cornerstone regulatory guidance for computerised systems
Applying ICH Q9 to Pharmaceutical Quality Systems
This practical online course moves beyond the theoretical principles of ICH Q9 to provide a hands-on framework for integrating Quality
Essential Calculations for Clinical Pharmacists
This intensive online course is designed for pharmacy professionals and students seeking to master the critical mathematical skills required for
Pharmacy Calculation and Compounding
This comprehensive online course is designed to build your confidence and competence in accurate calculation and safe compounding. Through detailed
DoE Application in Formulation Development
This course provides a step-by-step guide to designing, analyzing, and interpreting experiments for pharmaceutical formulations using DoE techniques. By efficiently
Fundamentals of Regulatory Writing
This course provides a foundational introduction to writing documentation that satisfies global health authorities, such as the FDA, EMA, PMDA,
Understanding Bioequivalence: From Theory to Regulatory Approval
This comprehensive course provides an in-depth exploration of bioequivalence (BE), a critical concept in pharmaceutical sciences that ensures generic drugs
Basics of eCTD Submission
This online course provides a clear and straightforward breakdown of the eCTD structure and submission process. Learn what the eCTD
Introduction to FDA 21 CFR Part 211
This online course outlines the Current Good Manufacturing Practices (cGMP) for pharmaceutical products. Participants will learn key regulatory requirements for
Regulatory Aspects of Dissolution Testing in Pharma Industry
Dissolution testing is a critical quality control tool in pharmaceutical industry, but its true value is unlocked only when it
Introduction to Antimicrobial Stewardship
This foundational course provides healthcare professionals with essential knowledge and practical strategies to implement effective Antimicrobial Stewardship (AMS) programs in
Basic GLP
This is a certification course on GLP containing basic knowledge of Good Laboratory Practice (GLP) in pharmaceutical industry with lifetime
Basic GMP
This is a certification course on GMP containing basic knowledge of Good Manufacturing Practice (GMP) in pharmaceutical industry with lifetime
Introduction to Pharmaceutical Quality Assurance
This course provides you a foundational understanding of Pharmaceutical Quality Assurance (QA), a critical function in ensuring the safety, efficacy,