LMS Training Portal
Access GMP training programs, review course details, and begin your learning journey.
Active Pharmaceutical Ingredients - WHO GMP
Covers GMP principles applicable to the manufacture and control of active pharmaceutical ingredients (APIs), including quality management, materials, facilities, equipment, production controls, laboratory operations, documentation, validation, change control, investigations, storage, and distribution of APIs.
Aseptic Behavior and Gowning Excellence Training
Advanced GMP training on aseptic behavior, gowning excellence, contamination control, and regulatory expectations.
Certified Aseptic Media Fill Specialist
The Certified Aseptic Media Fill Specialist program provides a comprehensive, practical, and regulatory-driven understanding of aseptic processing and media fill validation in sterile pharmaceutical manufacturing.
Complaints and Recalls - WHO GMP
Covers the GMP systems required for receiving, investigating, documenting, and trending product complaints and for effectively managing product recalls. Emphasis is placed on investigation, quality risk, traceability, corrective actions, regulatory responsibilities, and protection of patients.
Contract Production and Analysis - WHO GMP
Covers WHO GMP requirements for outsourced manufacturing and laboratory activities, including responsibilities of contract givers and contract acceptors, technical agreements, qualification and oversight of contractors, documentation, communication, and maintenance of GMP compliance for outsourced operations.
Data Integrity for Chromatographic Systems
Comprehensive training on ensuring data integrity in HPLC, GC, and chromatography systems aligned with FDA, MHRA, and EU GMP expectations.
Deviation, Investigation, CAPA, and Root Cause Analysis Training
A practical GMP course covering deviations, investigations, root cause analysis, CAPA development, effectiveness checks, and inspection readiness.
Equipment Requirements - WHO GMP
Covers WHO GMP principles for pharmaceutical manufacturing and laboratory equipment, including appropriate design, installation, qualification, operation, cleaning, maintenance, calibration, equipment status, documentation, and controls necessary to prevent contamination, errors, and product-quality failures.
GMP Data Integrity Fundamentals
Practical GMP data integrity training covering ALCOA+, audit trails, documentation practices, and inspection readiness.
GMP Documentation Management Training
GMP documentation and data integrity training.
Good Practices in Production and Quality Control - WHO GMP
Covers essential WHO GMP practices for pharmaceutical production and quality control, including authorized procedures, in-process controls, prevention of contamination and mix-ups, laboratory controls, sampling, testing, documentation, batch evaluation, and appropriate release of pharmaceutical products.
Human Error - The Leading Cause of GMP Failure
A practical GMP course focused on human error prevention, behavioral factors, system design, and strategies to reduce deviations and compliance failures.
Introduction to GMP - WHO
An introduction to the fundamental principles of Good Manufacturing Practices (GMP) based on WHO guidance, including the purpose of GMP, quality and patient-safety considerations, regulatory expectations, and the responsibilities of pharmaceutical manufacturers in consistently producing medicines of appropriate quality.
Material Requirements - WHO GMP
Covers GMP controls for pharmaceutical materials throughout their lifecycle, including receipt, identification, quarantine, sampling, testing, approval, storage, dispensing, handling, rejection, and traceability of starting materials, packaging materials, intermediates, bulk products, and finished products.
Media Fill Foundation Course
Basic of Media Fill activities
Out of Specification Management
GMP training course available in the Learn GMP LMS.
PIC/S GMP Fundamentals & Regulatory Framework
An overview of PIC/S GMP principles, regulatory framework, and the role of PIC/S in harmonizing pharmaceutical GMP standards worldwide.
PIC/S Personnel, Training & Hygiene
An overview of PIC/S GMP requirements for pharmaceutical personnel, training, responsibilities, competency, personal hygiene, and contamination prevention.
PIC/S Pharmaceutical Quality System & Management Responsibility
An overview of the PIC/S Pharmaceutical Quality System, management responsibilities, quality governance, and organizational accountability for GMP compliance.
Personnel Requirements - WHO GMP
Covers WHO GMP requirements for pharmaceutical personnel, including organizational responsibilities, qualifications, training, competency, hygiene, defined roles, supervision, and the responsibilities of key personnel involved in production, quality assurance, and quality control.
Pharmaceutical Change Control Management Training
A practical GMP course covering pharmaceutical change control lifecycle, impact assessment, cross-functional review, implementation, and effectiveness verification.
Premises Requirements - WHO GMP
Covers WHO GMP expectations for the location, design, construction, maintenance, and control of pharmaceutical premises. Key topics include material and personnel flows, prevention of contamination and mix-ups, production areas, storage areas, laboratories, and supporting facilities.
Qualification and Validation - WHO GMP
Covers the fundamental WHO GMP principles of qualification and validation, including facilities, utilities, equipment, processes, cleaning, analytical methods, documentation, validation planning, and maintaining validated systems throughout their lifecycle.
Quality Management - WHO GMP
This course is updated and enhanced to align with current regulatory expectations (ICH Q10, WHO GMP, EU GMP, FDA guidance), including: Clear hierarchy of Quality Management, Quality Assurance, GMP, and Quality Control Detailed QA system requirements (design, control, release, storage, distribution, self-inspection, change control, continuous improvement) Manufacturer's responsibility for safety, efficacy, and quality Basic GMP requirements (resources, documentation, validation, complaints, recalls) Updated case studies and common deficiencies
Quality Management - WHO GMP
Covers the essential principles of pharmaceutical quality management under WHO GMP, including quality assurance, GMP responsibilities, quality control, management commitment, documentation, product quality, and the systems required to maintain consistent compliance throughout pharmaceutical operations.
Quality Management System (Basic)
This comprehensive GMP Quality Management System (QMS) Training Course provides professionals working in pharmaceutical, biotechnology, medical device, and regulated healthcare industries with a practical understanding of modern quality systems required to ensure regulatory compliance, product quality, patient safety, and inspection readiness.
Sanitation and Hygiene - WHO GMP
Covers WHO GMP expectations for sanitation and hygiene in pharmaceutical manufacturing, including personnel hygiene, facility cleanliness, contamination prevention, cleaning practices, sanitation programs, and controls necessary to protect products from contamination and cross-contamination.
Self Inspection and Quality Audits - WHO GMP
Covers the principles and practices of GMP self-inspection and quality auditing, including audit planning, inspection techniques, identification and classification of deficiencies, reporting, corrective and preventive actions, follow-up, and continuous improvement of the pharmaceutical quality system.
Sterile Manufacturing: Aseptic Processing Course
A practical GMP training course on sterile manufacturing and aseptic processing.
Sterile Manufacturing: Principles, Compliance, and Best Practices
A practical GMP course covering sterile manufacturing fundamentals, contamination control, regulatory expectations, and best practices for aseptic operations.
Sterile Pharmaceutical Products - WHO GMP
Covers key GMP principles applicable to sterile pharmaceutical manufacturing, including contamination control, clean areas, environmental conditions, personnel practices, aseptic operations, sterilization, monitoring, validation, and controls necessary to maintain sterility assurance and protect product quality.
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