Colin Booth,Colin Booth, QMS - Quality Microbiology Solutions, UK
Dr Sven M. Deutschmann, Roche Diagnostics, Germany
Dr Marcel Goverde, MGP Consulting, Switzerland
Dr Holger Kavermann, Roche Diagnostics, Germany
Arjan Langen, MSD, The Netherlands
Most tests applied in microbiological QC are described in detail in the different Pharmacopoeias (e.g. EP, USP, and JP). These methods are regarded as being validated - but not for your products!
In the end, it is up to you to prove that the official methods function in your environment.
The validation of microbiological test methods for your needs consumes a lot of time, money and manpower. Things can get more complicated if your products interfere with the execution of the test.
The real challenge is to fulfil both, regulatory requirements and at the same time financial targets set by your management.
During this 3-day workshop you develop strategies for a sustainable approach perform microbiological test procedures in compliance with the regulations. This course will give you clear guidance on how to cope with these tasks besides your routine laboratory work.
The key tool of this seminar will be team work. During interactive sessions you will create procedures for the most common microbial test methods. Our experienced ECA course leaders will moderate the discussions to lead you to practice-oriented solutions.
After completion of the course you will be able to run microbiological test procedures in a compliant and at the same time efficient manner.
To guarantee optimal conditions for the exchange of opinions and experiences, the number of participants is limited!
This course will provide practical guidance on implementing the harmonized test methods as well as alternative microbiological methods
This GMP Workshop is designed for microbiologists, managers and supervisors of pharmaceutical microbiological laboratories.
Furthermore, the course will be of interest to personnel from quality control, quality assurance, regulatory affairs and contract laboratories involved in the microbiological aspects of the production and testing of medicinal products
Lab Layout and Equipment Qualification
Basic Requirements for Microbiological Laboratories
Method Suitability Test - Requirements and Materials
- Clean and dirty concepts
- Avoiding cross contamination
- Lay out requirements for a PCR Lab
- Equipment Qualification - Points to consider for a microbiological lab
Training and Qualification of Analysts
- Designing a MST strategy
- Worked examples of MST, creams, liquids, tablets
- Sterility test validation: why do so many laboratories get it wrong?
- MST for difficult formulations
- Validation and robustness are they the same thing?
- Transferring methods to other laboratories, what do you need?
- Microbial cultures, selection and maintenance
- Microbiological media: how to make it, store it and test it
A structured training programme for microbiologists what they need to know and why
Microbial Limit Test for Non-Sterile Products
Compliant Microbiological Test Methods
Bacterial Endotoxins/Test Validation
- The harmonised approach USP/Ph.Eur. /JP
- Relevant parameters in the test procedure
- Choosing the most suitable test method
- Microbial quality of excipients, API and final dosage forms
- Defining alert levels based on historical data
- The approach of risk assessment testing
The Test of Sterility: Critical Parameters for a Validation of the Test Procedures
- Principles of the techniques
- Gel-clot techniques
- Photometric techniques
- Preparatory testing / validation tests
Tests for Specified Microorganisms
- Validation tests
- Test procedures
- Membrane filtration method
- Direct transfer or direct inoculation method
Rapid Microbiological Methods
- Testing Methods
- Challenges concerning the suitability testing
- How to choose the right growth media supplier
- What are objectionable micro-organisms
The Paperless Lab
- Overview on the current RMMs
- Limitations and benefits of the different RMM?
- Registration of samples via an Intranet-based electronic form sheet
- eProtocol - avoiding paperbased recording)
- Integration of gadetry in the LIMS (e.g. MTP reader for kinetic-turbidimetric endotoxin test or Growth Direct)
- Monitoring of non-sterile processes
- Aseptic manufacture:
- developing a programme
- interpreting data
- regulatory requirements
- Monitoring methods; air, surface, people
- A complete programme for a sterile produc
The Real World - A Workshop Day
You will participate in 3 workshops!
These interactive sessions are an excellent forum for fruitful discussions. You will develop testing and validation strategies that can be transferred directly to your lab. The ECA course leaders take care that you stay focused on the pre-defined exercises.
The harmonized methods for testing of non-sterile Products
The goal of this workshop is encourage the participants to think globally when analysing microbiology problems. Microbiology problems are subtle and often multifactorial in their origin. The workshop will show you tips and tricks in testing methods and a possibility to discuss the issues of the implementation of the harmonized methods like growth promotion testing, creating an implementation concept and necessary investments.
Rapid Microbiological Methods
This workshop offers you a unique possibility to evaluate the new developments in RMM systems to extend the experiences in validation and implementation of these systems in pharmaceutical industry. Furthermore you will learn more about the expectations of European and US authorities.
Risk Assessment and Trending
This workshop will give you an insight in trending of microbiological data and principles of microbiological risk assessments. It will cover the regulatory background like ICH Q9 and make you familiar with risk identification tools like FMEA (Failure Mode and Effects Analysis) or FTA (Fault Tree Analysis)
The workshop gives you an understanding of how to set-up an environmental monitoring programme, and how to handle excursions. The discussions will focus on initial qualification vs routine monitoring, how many samples are reasonable, reporting structure of environmental monitoring data, corrective actions and the impact of environmental data on product release.
Identification Techniques - Phenotypic / Genotypic
Dealing with OOS-Results
- Phenotypic and genotypic identification techniques-advantages and limitations
- A change from phenotypic to genotypic identification and the surprises
- New Methods - what's in sight?
Disinfection - Efficacy Testing and Validation
- How do we define alert and action limits?
- How should we react on Out-Of-Specification results?
- How can we perform a proper Failure Investigation?
- Antimicrobial Agents and their Efficacy
- Testing Methods
- Efficacy testing against Isolates
- Validation approach
Method Validation According 5.1.6.
- Capturing changes in your process.
- When is a change not a change?
- Change control after the event!
- Your change control process, making it robust.
- Background of chapter Ph. Eur. 5.1.6
- Revision of chapter 5.1.6
- Validation process
- Accuracy, Precision, Specificity, LOD, LOQ, Linearity, Range, Robustness