TÜV SÜD Product Service is hosting two Medical Workshops in Fareham on 2nd and 3rd November 2011. The courses will be delivered by TÜV SÜD’s Medical & Health Service Specialist, Jeff Vest.
“Introduction to Microbiology for the Manufacture of Sterile Medical Devices / Products”, taking place at Octagon House, Fareham on 2nd November 2011, this course covers the fundamentals of microbiology as it applies to the medical devices, pharmaceutical and associated industries in a real world context to ensure that your product meets the requirements of the patient and of you, the manufacturer.
With over 20 years of experience of microbiology in the healthcare industries, our expert Jeff Vest, will reveal to our guests how to demystify the secrets to the “black art” of microbiology, use the data to conduct process improvements and about setting up a microbiological control program in order to add value.
Our second course on 3rdNovember will cover the fundamentals of the Medical Devices Directive (93/42/EEC as amended by council directive 2007/47/EC) and ISO 13485:2003 in a real world context to ensure that your product meets the requirements of the patient, you, the manufacturer and the regulatory authorities. Anyone with an interest in regulatory affairs, involved in the production of medical devices, technicians, supervisors and students could benefit from this course.
TÜV SÜD Product Service is the largest EU Notified Body for the Medical Devices Directive, with extensive experience in regulatory approvals. We provide a wide range of training services, sharing our expertise in product and quality system conformance.
Based on real life experiences, we provide you with valuable information in getting your products and services to market on a global basis.
To learn more please follow the link :
“Introduction to Microbiology for the Manufacture of Sterile Medical Devices / Products”, taking place at Octagon House, Fareham on 2nd November 2011, this course covers the fundamentals of microbiology as it applies to the medical devices, pharmaceutical and associated industries in a real world context to ensure that your product meets the requirements of the patient and of you, the manufacturer.
With over 20 years of experience of microbiology in the healthcare industries, our expert Jeff Vest, will reveal to our guests how to demystify the secrets to the “black art” of microbiology, use the data to conduct process improvements and about setting up a microbiological control program in order to add value.
Our second course on 3rdNovember will cover the fundamentals of the Medical Devices Directive (93/42/EEC as amended by council directive 2007/47/EC) and ISO 13485:2003 in a real world context to ensure that your product meets the requirements of the patient, you, the manufacturer and the regulatory authorities. Anyone with an interest in regulatory affairs, involved in the production of medical devices, technicians, supervisors and students could benefit from this course.
TÜV SÜD Product Service is the largest EU Notified Body for the Medical Devices Directive, with extensive experience in regulatory approvals. We provide a wide range of training services, sharing our expertise in product and quality system conformance.
Based on real life experiences, we provide you with valuable information in getting your products and services to market on a global basis.
To learn more please follow the link :
http://www.tuvps.co.uk/home_psuk/services/training
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Leaders in EMC Testing , Environmental Testing, Safety Testing, Radio and Telecoms Testing, CE Marking, Vibration Testing, Climatic Testing, Certification, Training and Consulting
Do you have a question ask it here?
Leaders in EMC Testing , Environmental Testing, Safety Testing, Radio and Telecoms Testing, CE Marking, Vibration Testing, Climatic Testing, Certification, Training and Consulting
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