Pharmaceutical training courses A to Z

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ATMP and Biotechnology

ATMPs Quality by design from bench to clinic
Good Clinical Practice specific to ATMPs
ATMP Webinar
QP Biotechnology Issues

Auditing

Active Pharmaceutical Ingredients Auditing
Auditing to Pharmaceutical Standards
IRCA GMP lead auditor (pharmaceutical quality systems) – PR325
GDP and RP Auditor
IRCA QMS lead auditor for the pharmaceutical supply chain (PS9000/ISO9001) – PR330
Management of GMP Inspections
Internal Auditor
eLearning - Auditing against the New Annex 1 Steriles Guideline CPD

eLearning

Good Manufacturing Practice
Good Distribution Practice
Introduction to Pharmaceutical Microbiology
Pharmaceutical Quality System (PQS)
Quality Risk Management
Introduction to pharmacovigilance
PQS - Audits and Self Inspections
PQS - Change Management and Control
PQS - Complaints Quality Defects and Product Recalls
PQS - Deviation and CAPA Management
eLearning - Auditing against the New Annex 1 Steriles Guideline CPD
PQS - Documentation
PQS - Management Review
PQS - People and Training
PQS - Product Quality Review
PQS - Supplier Management
PQS - Validation and Qualification
QP Active pharmaceutical ingredients - knowledge reinforcement
QP Investigational medicinal products - knowledge reinforcement
QP Medicinal chemistry and therapeutics - eLearning knowledge reinforcement
QP Pharmaceutical quality systems - eLearning knowledge reinforcement

GDP and Responsible Person

GDP and RP Auditor
Good Distribution Practice
Responsible Person and GDP, Cogent Gold Standard Approved
Responsible Person Refresher
Responsible Person Forum
Responsible Person Import: Role and Requirements
Good Distribution Practice (eLearning)

Good manufacturing practice

GAMP 5 Second Edition Workshop
Good Manufacturing Practice - Advanced - RSC Approved
Good Manufacturing Practice - The Essentials
Good Manufacturing Practice in the Laboratory
GxP Computerised Systems Validation and Compliance
Interpretation of Statistical Values Used in GMP Applications
Internal Auditor
Management of GMP Inspections
Medical Device Regulation (MDR) 2017/745
Pharmaceutical Product Development, GMP requirements
Pharmaceutical Quality Management System
Good Manufacturing Practice (eLearning)
Pharmaceutical Quality System (eLearning)

Microbiology

Environmental Monitoring - In Partnership with Cherwell Laboratories
Introduction to Pharmaceutical Microbiology
Manufacturing Sterile Products
Water Systems and Microbiological Control
Introduction to pharmaceutical microbiology (eLearning)

Qualified person

Active Pharmaceutical Ingredients
Analysis and Testing
Biotechnology Issues
Investigational Medicinal Products
Mathematics and Statistics
Medicinal Chemistry and Therapeutics
Pharmaceutical Formulation and Processing Part 1
Pharmaceutical Formulation and Processing Part 1 - Practical laboratory day
Pharmaceutical Formulation and Processing Part 2
Pharmaceutical Law and Administration
Pharmaceutical Microbiology
Pharmaceutical Packaging
Pharmaceutical Quality Systems
Role and Professional Duties
QP Expert Consultation 1 to 1
QP Viva Preparation Day
QP or Not to QP a webinar for aspiring QPs
eLearning QP Knowledge Reinforcement Modules
QP Group Mentoring
QP Hot Topic WebTorial
Responsible Person and GDP Cogent approved
IRCA Lead Auditor Courses
Leadership and Influencing Skills for QPs
QC Chemistry Crash Course
Introduction to Pharmaceutical Microbiology
Interpretation of Statistical Values used in GMP Applications
Key Regulatory Updates for the Pharma Industry
QP Workshop

Validation

Cleaning Validation
Introduction to Validation
GAMP 5 Second Edition Workshop
GxP Computerised Systems Validation and Compliance
Process Validation & Qualification, including Validation Methods

Others

Data Integrity and Electronic Records and Signatures
Introduction to Pharmacovigilance
Leadership and Influencing Skills for New Managers
Quality Risk Management - How to apply ICH Q9 in Practice
QC Chemistry - Crash Course
GAMP 5 Second Edition Workshop
QP Pharmaceutical Packaging
Root Cause Analysis & CAPA
Technical Report Writing
Technology Transfer of Pharmaceutical Products
Quality Risk Management (eLearning)

Webinars

ATMP Webinar
Key Regulatory Updates for the Pharma Industry
QP Hot Topic WebTorial
QP or Not to QP a webinar for aspiring QPs
Responsible Person Forum

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