LMS Training Portal
Access GMP training programs, review course details, and begin your learning journey.
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Active Pharmaceutical Ingredients - WHO GMP
What You Will Learn
Understand GMP requirements for API manufacturing, including quality management, material controls, facilities and equipment, production, laboratory operations, documentation, validation, investigations, change control, storage, and distribution.
Who Should Take This Course
QA, QC, Production, Engineering, Validation, Regulatory Affairs, warehouse, and other personnel involved in API manufacturing, testing, storage, distribution, or oversight.
1 Modules
•
1 Lessons
Premium
$149.00
Aseptic Behavior and Gowning Excellence Training
What You Will Learn
Apply appropriate aseptic behavior, gowning practices, personnel qualification, contamination-control principles, cleanroom discipline, and intervention controls required for compliant sterile manufacturing operations.
Who Should Take This Course
Aseptic operators, sterile manufacturing personnel, QA, QC microbiology, trainers, supervisors, and employees entering or supporting classified and aseptic processing areas.
6 Modules
•
18 Lessons
Premium
$149.00
Certified Aseptic Media Fill Specialist
What You Will Learn
Understand aseptic processing and media fill requirements, including study design, execution, interventions, contamination control, environmental monitoring, investigations, interpretation of results, and regulatory expectations for demonstrating sterility assurance.
Who Should Take This Course
Aseptic manufacturing, QA, validation, microbiology, production supervision, contamination control, and personnel responsible for media fill programs.
9 Modules
•
50 Lessons
Free
Free
Complaints and Recalls - WHO GMP
What You Will Learn
Manage pharmaceutical complaints and recalls using appropriate investigation, documentation, traceability, risk assessment, corrective action, regulatory communication, recall execution, and effectiveness controls to protect patients.
Who Should Take This Course
QA, Quality Systems, Regulatory Affairs, Production, warehouse, distribution, customer complaint personnel, and professionals involved in complaint investigations or product recalls.
1 Modules
•
1 Lessons
Free
Free
Contract Production and Analysis - WHO GMP
What You Will Learn
Understand WHO GMP requirements for outsourced manufacturing and testing, including contractor qualification, technical agreements, responsibilities, oversight, documentation, communication, performance monitoring, and maintenance of GMP compliance.
Who Should Take This Course
QA, QC, Procurement, Supply Chain, Regulatory Affairs, contract manufacturing teams, laboratory management, and personnel responsible for outsourced GMP activities.
1 Modules
•
1 Lessons
Premium
$149.00
Data Integrity for Chromatographic Systems
What You Will Learn
Apply data integrity principles to HPLC, GC, CDS, and chromatographic records, including audit trails, user access, integration controls, electronic records review, and regulatory inspection readiness.
Who Should Take This Course
QC analysts, laboratory supervisors, QA reviewers, IT/CSV, system administrators, validation personnel, and professionals responsible for chromatographic data and computerized laboratory systems.
5 Modules
•
20 Lessons
Free
Free
Deviation, Investigation, CAPA, and Root Cause Analysis Training
What You Will Learn
Manage deviations through structured investigation, root cause analysis, risk assessment, CAPA development, implementation, effectiveness verification, documentation, trending, and inspection-ready investigation practices.
Who Should Take This Course
QA, QC, Production, Engineering, Validation, laboratory personnel, investigators, supervisors, and professionals involved in deviations, investigations, CAPA, or root cause analysis.
7 Modules
•
21 Lessons
Free
Free
Equipment Requirements - WHO GMP
What You Will Learn
Apply WHO GMP requirements for equipment design, installation, qualification, operation, cleaning, maintenance, calibration, status control, documentation, and prevention of contamination, errors, and product-quality failures.
Who Should Take This Course
Engineering, Maintenance, Validation, Production, QA, QC, calibration personnel, equipment owners, and professionals responsible for GMP manufacturing or laboratory equipment.
1 Modules
•
1 Lessons
Free
Free
GMP Data Integrity Fundamentals
What You Will Learn
Apply ALCOA+ principles to GMP records and electronic data, recognize common data integrity risks, understand audit trail expectations, and strengthen documentation practices and inspection readiness.
Who Should Take This Course
QA, QC, laboratory, manufacturing, IT/CSV, validation, data owners, reviewers, and personnel who create, process, review, or approve GMP data.
6 Modules
•
19 Lessons
Free
Free
GMP Documentation Management Training
What You Will Learn
Apply Good Documentation Practices and ALCOA+ principles to GMP documents and records, including document creation, review, approval, issuance, revision, retention, archival, and data integrity controls.
Who Should Take This Course
QA, QC, Production, laboratory, Validation, Engineering, Regulatory Affairs, document control personnel, and anyone who creates, reviews, approves, or maintains GMP records.
7 Modules
•
21 Lessons
Free
Free
Good Practices in Production and Quality Control - WHO GMP
What You Will Learn
Apply WHO GMP practices to pharmaceutical production and Quality Control, including approved procedures, in-process controls, contamination prevention, laboratory testing, sampling, documentation, batch evaluation, and product release.
Who Should Take This Course
Production, QA, QC, laboratory, manufacturing supervisors, batch reviewers, and professionals responsible for pharmaceutical manufacturing, testing, documentation, or product release.
1 Modules
•
1 Lessons
Free
Free
Human Error - The Leading Cause of GMP Failure
What You Will Learn
Recognize human error types and contributing factors, evaluate error-prone systems and behaviors, investigate underlying causes, and apply practical controls that reduce recurrence and strengthen GMP performance.
Who Should Take This Course
QA, Production, QC, supervisors, trainers, investigators, process owners, and personnel responsible for preventing human-error-related GMP deviations and compliance failures.
7 Modules
•
21 Lessons
Free
Free
Introduction to GMP - WHO
What You Will Learn
Understand the purpose and fundamental principles of WHO GMP, including patient protection, product quality, manufacturer responsibilities, regulatory expectations, contamination prevention, documentation, and consistent control of pharmaceutical operations.
Who Should Take This Course
Pharmaceutical employees, new GMP personnel, QA, QC, Production, Engineering, warehouse staff, supervisors, and professionals requiring an introduction to WHO GMP.
1 Modules
•
1 Lessons
Free
Free
Material Requirements - WHO GMP
What You Will Learn
Apply GMP controls throughout the material lifecycle, including receipt, identification, quarantine, sampling, testing, approval, storage, dispensing, handling, rejection, and traceability of pharmaceutical materials and products.
Who Should Take This Course
Warehouse, Supply Chain, Production, QA, QC, dispensing, sampling, materials management personnel, and professionals responsible for handling or controlling GMP materials.
1 Modules
•
1 Lessons
Free
Free
Media Fill Foundation Course
What You Will Learn
Understand the purpose and basic principles of media fill studies, including aseptic process simulation, study preparation, interventions, incubation, acceptance criteria, contamination evaluation, and documentation.
Who Should Take This Course
Aseptic operators, QA, microbiology, validation, production supervisors, and personnel who need a foundational understanding of media fill activities.
1 Modules
•
5 Lessons
Free
Free
Out of Specification Management
What You Will Learn
Understand the management of out-of-specification results, including initial laboratory assessment, investigation strategy, hypothesis testing, manufacturing investigation, root cause evaluation, CAPA, documentation, and regulatory expectations.
Who Should Take This Course
QC analysts, laboratory supervisors, QA, Production, investigators, reviewers, and personnel responsible for evaluating, investigating, approving, or trending OOS results.
12 Modules
•
12 Lessons
Premium
$149.00
PIC/S GMP Documentation & Data Integrity
What You Will Learn
Understand PIC/S expectations for GMP documentation, recordkeeping, good documentation practices, document control, data integrity, ALCOA+ principles, electronic records, and inspection readiness.
Who Should Take This Course
QA, QC, production, laboratory, warehouse, validation, engineering, regulatory, documentation personnel, supervisors, managers, and other personnel responsible for creating, reviewing, approving, maintaining, or inspecting GMP records.
6 Modules
•
12 Lessons
Free
Free
PIC/S GMP Fundamentals & Regulatory Framework
What You Will Learn
Understand the PIC/S organization, regulatory framework, GMP Guide, inspection philosophy, international cooperation, and the role of PIC/S in harmonizing pharmaceutical GMP standards and regulatory expectations.
Who Should Take This Course
QA, QC, Production, Validation, Engineering, Regulatory Affairs, auditors, managers, and pharmaceutical professionals seeking an introduction to PIC/S GMP requirements.
7 Modules
•
7 Lessons
Premium
$149.00
PIC/S Personnel, Training & Hygiene
What You Will Learn
Understand PIC/S requirements for personnel responsibilities, qualifications, GMP training, competency, health, personal hygiene, gowning, contamination prevention, supervision, and behaviors that support pharmaceutical product quality.
Who Should Take This Course
Production, QA, QC, warehouse, laboratory, supervisors, trainers, managers, and personnel working in or supporting GMP-controlled pharmaceutical operations.
6 Modules
•
12 Lessons
Premium
$149.00
PIC/S Pharmaceutical Quality System & Management Responsibility
What You Will Learn
Understand PIC/S Pharmaceutical Quality System principles, including management responsibility, quality policy and objectives, Quality Risk Management, CAPA, change management, Product Quality Review, management review, and continual improvement.
Who Should Take This Course
QA, Quality Systems, Production, QC, Validation, Engineering, Regulatory Affairs, supervisors, managers, and personnel responsible for pharmaceutical quality governance and PIC/S compliance.
6 Modules
•
12 Lessons
Premium
$149.00
PIC/S Premises, Facilities & Equipment
What You Will Learn
Understand PIC/S requirements for pharmaceutical premises, facility design, production and storage areas, equipment design and installation, cleaning, utilities, preventive maintenance, qualification, contamination prevention, and GMP inspection readiness.
Who Should Take This Course
Production, engineering, maintenance, validation, QA, QC, warehouse, facilities, utilities, supervisors, managers, and personnel responsible for GMP-controlled pharmaceutical premises and equipment.
6 Modules
•
12 Lessons
Premium
$149.00
PIC/S Production & Manufacturing Controls
What You Will Learn
Understand PIC/S requirements for pharmaceutical production, materials management, manufacturing instructions, in-process controls, prevention of mix-ups and cross-contamination, packaging and labeling controls, yield reconciliation, deviations, and maintaining controlled production operations.
Who Should Take This Course
Production, manufacturing, packaging, warehouse, QA, QC, engineering, validation personnel, supervisors, managers, and other personnel responsible for GMP-controlled pharmaceutical manufacturing operations.
6 Modules
•
12 Lessons
Premium
$149.00
PIC/S Quality Control & Laboratory GMP
What You Will Learn
Understand PIC/S requirements for pharmaceutical Quality Control, GMP sampling, specifications, laboratory testing, equipment and instruments, laboratory documentation, data integrity, OOS investigations, stability programs, reference samples, QC review, and inspection readiness.
Who Should Take This Course
QC analysts, laboratory personnel, QA personnel, microbiologists, chemists, supervisors, laboratory managers, validation personnel, manufacturing personnel, and others responsible for GMP laboratory operations and quality decisions.
6 Modules
•
12 Lessons
Free
Free
Personnel Requirements - WHO GMP
What You Will Learn
Understand WHO GMP personnel requirements for organizational responsibilities, qualifications, training, competency, hygiene, supervision, defined roles, and responsibilities of key Production, Quality Assurance, and Quality Control personnel.
Who Should Take This Course
Pharmaceutical employees, managers, supervisors, QA, QC, Production personnel, trainers, HR training coordinators, and individuals responsible for GMP competency and personnel compliance.
1 Modules
•
1 Lessons
Premium
$149.00
Pharmaceutical Change Control Management Training
What You Will Learn
Apply the pharmaceutical change control lifecycle, including change initiation, classification, risk and impact assessment, cross-functional review, implementation, validation linkage, effectiveness verification, and regulatory compliance.
Who Should Take This Course
QA, Production, QC, Validation, Engineering, Regulatory Affairs, IT/CSV, and personnel responsible for evaluating, approving, implementing, or reviewing GMP changes.
7 Modules
•
21 Lessons
Free
Free
Premises Requirements - WHO GMP
What You Will Learn
Understand WHO GMP requirements for pharmaceutical premises, including facility location, layout, design, maintenance, personnel and material flow, production areas, storage, laboratories, and prevention of contamination and mix-ups.
Who Should Take This Course
Engineering, Facilities, QA, Production, warehouse, Validation, project teams, maintenance personnel, and professionals involved in pharmaceutical facility design or operation.
1 Modules
•
1 Lessons
Free
Free
Qualification and Validation - WHO GMP
What You Will Learn
Understand WHO GMP qualification and validation principles for facilities, utilities, equipment, processes, cleaning, analytical methods, documentation, validation planning, and lifecycle maintenance of validated systems.
Who Should Take This Course
Validation, QA, Engineering, Production, QC, maintenance, laboratory personnel, project teams, and professionals responsible for qualified equipment or validated GMP processes.
1 Modules
•
1 Lessons
Premium
$149.00
Quality Management - WHO GMP
What You Will Learn
Understand WHO GMP quality management principles, including Quality Assurance, GMP, Quality Control, management responsibility, quality systems, documentation, change control, self-inspection, continual improvement, and product quality oversight.
Who Should Take This Course
Pharmaceutical QA, QC, Production, Validation, Engineering, Regulatory Affairs, supervisors, managers, and personnel responsible for implementing or overseeing WHO GMP quality systems.
4 Modules
•
19 Lessons
Free
Free
Quality Management - WHO GMP
What You Will Learn
Understand WHO GMP pharmaceutical quality management principles, including Quality Assurance, GMP responsibilities, Quality Control, management commitment, documentation, product quality, and systems required for sustained compliance.
Who Should Take This Course
QA, QC, Production, Validation, Engineering, Regulatory Affairs, supervisors, managers, and personnel supporting pharmaceutical quality management systems.
1 Modules
•
1 Lessons
Free
Free
Quality Management System (Basic)
What You Will Learn
Understand the fundamental elements of a pharmaceutical Quality Management System, including quality governance, documentation, risk management, CAPA, change control, management oversight, continuous improvement, and inspection readiness.
Who Should Take This Course
QA, QC, Production, Validation, Engineering, Regulatory Affairs, supervisors, managers, and professionals seeking a foundational understanding of pharmaceutical quality systems.
1 Modules
•
1 Lessons
Free
Free
Sanitation and Hygiene - WHO GMP
What You Will Learn
Apply WHO GMP sanitation and hygiene principles for personnel, premises, equipment, cleaning, contamination prevention, sanitation programs, and controls designed to prevent product contamination and cross-contamination.
Who Should Take This Course
Production operators, QA, QC, sanitation personnel, Engineering, warehouse staff, supervisors, and employees working in pharmaceutical manufacturing or controlled areas.
1 Modules
•
1 Lessons
Free
Free
Self Inspection and Quality Audits - WHO GMP
What You Will Learn
Plan and conduct GMP self-inspections and quality audits, identify and classify deficiencies, document findings, evaluate CAPA responses, perform follow-up, and use audit results to support continual improvement.
Who Should Take This Course
Quality auditors, QA, QC, Production, supervisors, department managers, compliance professionals, and personnel participating in internal GMP audits or self-inspections.
1 Modules
•
1 Lessons
Premium
$149.00
Sterile Manufacturing: Aseptic Processing Course
What You Will Learn
Understand aseptic processing principles, cleanroom controls, personnel practices, environmental monitoring, contamination risks, media fills, investigations, CAPA, and batch release considerations in sterile manufacturing.
Who Should Take This Course
Aseptic manufacturing personnel, QA, QC microbiology, validation, engineering, supervisors, and professionals involved in sterile product manufacturing and oversight.
10 Modules
•
30 Lessons
Premium
$149.00
Sterile Manufacturing: Principles, Compliance, and Best Practices
What You Will Learn
Understand sterile manufacturing principles, contamination control, cleanroom practices, environmental monitoring, aseptic operations, personnel behavior, investigations, and regulatory expectations necessary to maintain sterility assurance.
Who Should Take This Course
Sterile manufacturing operators, QA, QC microbiology, validation, engineering, supervisors, and professionals supporting aseptic or sterile manufacturing operations.
7 Modules
•
21 Lessons
Free
Free
Sterile Pharmaceutical Products - WHO GMP
What You Will Learn
Understand WHO GMP requirements for sterile pharmaceutical products, including clean areas, contamination control, environmental monitoring, personnel practices, aseptic operations, sterilization, validation, and controls supporting sterility assurance.
Who Should Take This Course
Sterile manufacturing personnel, QA, QC microbiology, Validation, Engineering, environmental monitoring teams, supervisors, and professionals supporting sterile pharmaceutical operations.
1 Modules
•
1 Lessons
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