Environmental Monitoring - Live Online Training
Compliant and Reasonable
Seminar Nr. 21006
This course is part of the GMP Certification Programme "ECA Certified Sterile Production Manager". Learn more.
Note: All times mentioned are CEST.
Unser Seminarservice
Kosten
| ECA-Member*: | EUR 1690,-- |
| Non ECA Member*: | EUR 1890,-- |
| EU/GMP Inspectorates*: | EUR 945,-- |
| APIC Member Discount*: | EUR 1790,-- |
Alle Preise zzgl. MwSt. Wichtige Hinweise zur Umsatzsteuer.
* auch unkompliziert per Kreditkarte bezahlbar
Rückfragen unter:
Tel.: 06221 / 84 44 0 E-Mail: info@concept-heidelberg.de
Sprecher
Arjan Langen, GE Healthcare, The Netherlands
Chris Randell, CooperVision, UK
Dr Björn Wiese, Janssen Cilag, Switzerland
Chris Randell, CooperVision, UK
Dr Björn Wiese, Janssen Cilag, Switzerland
Zielsetzung
Environmental monitoring is one of the systems that decide about the product quality in the manufacture of sterile medicinal products. Both European and American GMP regulations place special focus on this topic.
The USP 1116, the new EU GMP Annex 1 and especially the FDA’s “Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing - Current Good Manufacturing Practice“ deal in detail with environmental monitoring.
However, many of the requirements laid down in these documents seem to be excessive for everyday practice on the one hand and leave great scope for interpretation on the other hand.
In practice, environmental monitoring programmes sometimes develop into time-consuming, cost- and personnel-intensive measures. Therefore, it is the aim of this Live Online Training to provide the participants with pragmatic recommendations for the creation and implementation of environmental monitoring programmes.
Within the framework of this Live Online Training, the participants are confronted with current hot topics, like:
The USP 1116, the new EU GMP Annex 1 and especially the FDA’s “Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing - Current Good Manufacturing Practice“ deal in detail with environmental monitoring.
However, many of the requirements laid down in these documents seem to be excessive for everyday practice on the one hand and leave great scope for interpretation on the other hand.
In practice, environmental monitoring programmes sometimes develop into time-consuming, cost- and personnel-intensive measures. Therefore, it is the aim of this Live Online Training to provide the participants with pragmatic recommendations for the creation and implementation of environmental monitoring programmes.
Within the framework of this Live Online Training, the participants are confronted with current hot topics, like:
- Alert / action levels
- Relationship to batch release
- Locations and frequency
- Identification of isolates
- Sampling procedures
and get to know solutions for their own company practice.
Zielgruppe
This Live Online Training is directed at staff from Production, Quality Assurance and Quality Control who is responsible for the planning and implementation of environmental monitoring programmes.
It is also valuable for decision makers who have to deal with environmental monitoring data within the framework of product release.
It is also valuable for decision makers who have to deal with environmental monitoring data within the framework of product release.
Technical Requirements
We use Webex for our live online training courses and webinars. At www.gmp-compliance.org/training/online-training-technical-information you will find all the information you need to participate in our events and you can check if your system meets the necessary requirements to participate. If the installation of browser extensions is not possible due to your rights in the IT system, please contact your IT department. Webex is a standard nowadays and the necessary installation is fast and easy.
Programm
Environmental Monitoring
- Why do we do it – what does it tell us?
Relevant Guidelines
- The new EU-GMP Guide Annex 1
- USP <1116>
- FDA Aseptic Processing Guide
- ISO 14644 and ISO13824
- An overview about the most important guidances
Surface / Personnel Monitoring
- Surface:
- How?
- Surface sampling techniques
- Limitations
- Validation?
- Personnel:
- When and how?
- Results and specifications
- How to deal with shedders/pathogen carriers.
Viable Air Monitoring
- Regulatory Standards
- Settle Plates
- Validation
- Drying Issues
- Where to place them?
- Active Air Sampling
- Equipment options / comparison
- Validation
- Where to place them?
Clean Rooms – RABS – Isolator: Points to consider in Environmental Monitoring
- Comparison of the technical concepts
- Validation of microbiological media for the isolator
- Selection of sampling points
- Transfer of microbiological media
- Interpretation of the results and handling of excursions
Non-viable (particulate) Air Monitoring
- The grading of areas for manufacture of sterile medicinal products in the EU
- How to claim classification of areas to current standards
- How to ensure continuing compliance with the classification
- Selection of sampling locations for qualification and routine
- Particle monitoring, how and how often
- Handling the data
Workshop / Case Study: How to Establish an Environmental Monitoring Programme / Use of FMEA to Determine Sample Points in Routine Monitoring
- Identifying weaknesses in contamination control systems
- Identifying locations which will provide “early warning” signals of loss of control
- Preparing useful environmental monitoring SOPs
- Keeping manageable records
Case Study: Trending of Environmental Monitoring Data
- What is a trend?
- How can I use electronic systems to track and trend EM data?
- How to get meaningful information from trending
- Alert and action level setting
- Using trending as tool for pro-active environmental control measures
Microbiological Methods
- Microbiological media, growth requirements
- Identification of isolates
- Validating your methods
- Using rapid identification techniques
- Recovery problems
- Identification to the level of DNA, what value does it bring
Environmental Monitoring for Medical Devices
- Environmental Monitoring requirements considering ISO and AAMI
- Classified Cleanrooms
- Controlled Environment
- Real life example
- What to do when excursions occur?
Environmental Monitoring for Non-Steriles
- Why monitor non-sterile areas
- Risk vs impact
- Overview of regulatory position
- Case study
Deviation Management for Environmental Monitoring
- Steps to be taken in case of excursions
- When is an excursion a deviation?
- Comprehensive root cause analysis
- The nasty “re-occurrence”
- Finding of appropriate actions
Workshop / Case Study: Interpretation of OOS Results
- What is an OOS in environmental monitoring?
- OOS in relation to trends
- How to investigate
- Follow-up and corrective actions
- Consequences for batch release
Investigations / Documentation
- The information content of “variable” data versus quantitative limits
- Published and practical limits
- The information content of qualitative data
- Communicating with technical management and higher management
GMP Seminare nach Thema
- Allgemeine QA Themen + GMP Compliance
- Regulatory Affairs
- Development
- Datenintegrität
- Analytik allgemein
- Good Distribution Practice
- Computervalidierung
- Validierung allgemein
- Pharma Engineering allgemein
- API/Wirkststoffe/Hilfsstoffe
- Medizinprodukte und Combination Products
- GMP Grundlagen / Basis-Seminare
- Verpackung und Packmittel
- Hygiene
- Biotechnologie/Blut/ATMP
- Sachkundige Person (QP)
- European Conferences and Education Courses
- Sonstiges
- GMP Audits
- Dokumentation
- Reinigungsvalidierung
- IT allgemein
- Verunreinigungen/Impurities
- OOS / OOT / OOE
- Rohstoff-Prüfung
- Methodenvalidierung
- Gerätequalifizierung
- Stabilitätsprüfung
- Allgemeine mikrobiologische Themen
- Mikrobiologische Tests
- Technik
- Herstellung allgemein
- Sterile Herstellung
- Feste/halbfeste Formen
- Phytopharmaka/Cannabis/Radiopharmazeutika