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Pharmig Meetings Explore Current Topics in Pharmaceutical Microbiology
 | Pharmig have organised the following three meetings which help address the current needs of those working in or have responsibility for pharmaceutical microbiology.
| Risk Based Management in Pharmaceutical Microbiology
24th April, 2008, Liverpool, UK
Risk assessment and risk based management are current buzz phrases although not a new concept. The approaches of risk assessment and risk based management within microbiology merely formalise many of the activities that microbiologists have been undertaking for years. However, a formalised approach is now expected by the regulatory authorities! Sessions covered at this meeting include: - Risk Assessment and the Risk Management Process
- Regulatory Views and Guidelines on Risk Management
- Risk Assessment and Risk Management Methodologies
- Applying Failure Mode Effect Analysis (FMEA) to a Sterility Testing Isolator: A Case Study
- Risk Analysis using HACCP- A Microbiological Case Study
- Pharmaceutical Risk Management - an NHS Perspective
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Pharmig Summer Conference
21st - 22nd May, 2008, Cork, Ireland
Latest Updates and Hot Topics in Microbiology including: - Key note session from ex IMB speaker on 'Hot Topics for Regulators'
- Case Study: Recovery of Environmental Monitoring following Planned/Unplanned Shutdowns
- Manufacturing Investigations - What are the Regulators looking for?
- Managing the Risk of Human Error
- Risk Management of Contamination (RMC) During Manufacturing Operations in Cleanrooms
- Visions and Nightmares of a Microbiologist - Where Do We Go In Microbiological Quality Assurance?
- Harmonisation of Pharmacopoeial Methods and Implementation of Timing
- What the Company Microbiologist needs to know about Pharmaceutical Legislation and the Duties of the QP
- Parametric Release
- The Challenges of Microbiology in Blood Transfusion
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Setting up and Managing a Training Programme
18th June, 2008, Hertfordshire, UK
Are you in control of your training programme? Do you feel confident that it will meet regulatory scrutiny?
Microbiology training programmes are coming under increasing regulatory examination. Coupled with this - it is vital that companies also have a well-documented training system to meet GMP guidelines.
Unique to Pharmig, this hands on one-day workshop will ensure that you will leave with a clear understanding of the structure of a regulatory acceptable and compliant training programme.
This meeting is not lecture led. You, as delegates, will be presented with training files in which the practical workshop will be based around. In having open and frank discussions you will also be in the position to benchmark your current training programme with your peers, taking on board their approaches and structures as well as gaining a vital insight, from experienced tutors, into basic microbiological techniques which are often overlooked as an important part of a training programme.
Who Should Attend?
Managers/Supervisors in Microbiology QA/QC, Regulatory Training, Experienced Microbiology laboratory personnel.
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Source: Pharmig (Pharmaceutical Microbiology Interest Group)
Posted: April 2, 2008
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