GMP for Beginners
Understanding the Importance of GMP
Im Auftrag der ECA Academy

GMP for Beginners Understanding the Importance of GMP Im Auftrag der ECA Academy

Berlin, Germany

Seminar Nr. 17433




Bitte kontaktieren Sie uns und wir informieren Sie:

Rückfragen unter:
Tel.: 06221 / 84 44 0 E-Mail:


Dr Bettina Pahlen, Quality x Pharma Consulting
Dr Heinrich Prinz, PDM Consulting
Dr Wolfgang Schumacher, formerly F. Hoffmann-La Roche


The course is designed for people who have no or Little knowledge of GMP.
  • You get to know the most important pharmaceutical regulations and their importance,
  • you get a basic overview of GMP requirements in pharmaceutical production, and
  • you become familiar with technical terms from the field of GMP and their meaning


In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect for manufacturing high-quality products. For this reason, every staff member in the pharmaceutical industry has to be familiar with the basic GMP requirements. The relevant European GMP regulations define the following prerequisites:

Commisson directive 2003/94/EC
The personnel shall receive initial and ongoing training, the effectiveness of which shall be verified, covering in particular the theory and application of the concept of quality assurance and good manufacturing practice ….

EudraLex Vol. 4 Good manufacturing practice (GMP) guidelines
2.9 Besides the basic training on the theory and practice of Good Manufacturing Practice, newly recruited personnel should receive training appropriate to the duties assigned to them…..

In practice, many members of staff are often unaware of the contents and meaning of the different GMP requirements from Europe and US and their consequences for product quality. During this course, speakers with long-standing experience in the training of employees introduce and explain the most important elements of a pharmaceutical GMP system in an easy-to-understand way.


The course is directed to staff from the pharmaceutical industry having no or little experience with the current GMP requirements. This includes both employees who, after their vocational training, enter the pharmaceutical industry and experienced colleagues who work for the first time in a GMP-regulated environment. Participation is also recommended for personnel from suppliers who have to understand the quality requirements of their customers.


GMP: where do we come from - where do we go to?
  • Development of GMPs
  • GMP: Goal and general ideas
  • Types of regulatory documents and their meaning
  • GMP regulation for APIs, medicinal products and excipients - a comparison
  • Authorities and industry groups: ICH, PIC/S, EMEA, FDA, WHO, APIC, ISPE, IPEC
GMP in the US
  •  Comparison of  US and EU regulations
  •  Differences between European and FDA view on GMP / GMP vs cGMP
  •  Typical expectations of FDA and European inspectors
Quality Management System
  • Quality Management System cited in the regulations
  • General aspects of Quality Assurance
  • How to implement and structure a system
  • Responsibilities
Personnel and Training
  •  General aspects
  •  Qualification
  •  Key personnel
  •  Job descriptions
  •  Training (purpose, goals, contents, target groups)
  •  Planning and documentation of training
Hygiene / Personal Hygiene
  •  General aspects and rules
  •  Hygiene program
  •  Personnel flow
  •  Medical examination
  •  Contamination
  •  Monitoring
  •  Structure of documentation
  •  Responsibilities for the documentation
  •  SOP
  •  Documentation in the manufacturing process
  •  Documentation in the quality control
  •  Batch record review
  •  Annual report / Product quality report
  •  Specifications
Specific aspects of a QA System
  •  Deviations
  •  CAPA
  •  Change Control
  •  OOS
  •  Failure Investigations
  •  Self-inspections
Risk Management
  •  Main topics of ICH Q 9 / Part 3 EU GMP Guideline
  •  Risk management tools
  •  Use of risk analysis during qualification
  •  How to handle FMEA?
Premises / Production
  •  Requirements for room and equipment
  •  Classification of rooms
  •  Sterile production/isolator
  •  Maintenance of hygiene
  •  How to behave during production
  •  Definitions: Qualification, validation, calibration, maintenance, risk analysis
  •  Organizing qualification and validation: the validation master plan (VMP)
  •  Steps in Qualification studies: DQ, IQ, OQ, PQ
  •  Qualification parameters of typical types of equipment: Clean rooms, water systems, production equipment, analytical equipment
  •  Performing risk analysis: tools and practical tips
  •  Calibration: critical types of equipment
  •  How to build up a calibration system
  •  Maintenance: Requirements and system
  •  Validation of computerised systems
Process Validation, Computer Validation and Validation of Analytical Methods
  •  General aspects and requirements
  •  Process Validation
  •  Documentation of process validation
  •  Validation of analytical methods
  •  Documentation of analytical methods validation
Cleaning Validation
  •  Regulators requirements
  •  The cleaning procedure
  •  Building up a cleaning validation
  •  Sampling
  •  Analytical tests
Audits and Inspections
  •  Types of audits
  •  Requirements
  •  Dos and don’ts for the auditee - How to survive audits?
  •  Performing audits and self-inspections
  •  Good audit practices
  •  Packaging/Storage/Transportation in the regulations
  •  Managing of packaging process
  •  What is necessary to regulate in a pharmaceutical company
  •  WHO good storage practice – elements and requirements
  •  Transportation as part of storage
  •  How to maintain the quality during transportation
Falsified Products
  •  Regulatory requirements
  •  Responsibilities of QP and the pharmaceutical industry
  •  What measurements can be taken
  •  Strategies against falsified products


GMP Seminare nach Thema

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