Eo Sterilization Confirm And Routine Control Training - Chinaprice: contact company for price
Help enterprises make a better understanding on the specifications and regulations which are about requirements on special procedure conformation.
Detail introduction about medical device packing, technique of sterilization, materials used in medical packing and packing equipments.
Let people who take part in the training have a comprehensive understanding on this field.
1. Sterilization medical device packing training
Related standard regulations
Common packing forms
Basic principles and requirements
Basic requirements of packing materials
Basic performing experiment on packing system
Effective design methods
2. Training on EO Sterilization confirm
Introduction on EO sterilization
Technique and regulation challenge
Procedures on sterilization validation
3. Training on routine control
Training time and place:
Time: September 2012
Place: Guangzhou, specific time is undetermined
Introduction of organizers
Guangdong Medical Device Quality Supervision and Test Institute
Guangdong Medical Device Quality Supervision and Test Institute was founded in1988, directly affiliated institution of Food and Drug Administration, the only national medical equipment inspection institution in southern China as well as the medical device equipment quality supervision and inspection laboratory which is appointed by the State Food and Drug Administration. It performs the duties of Guangdong province quality supervision and medical equipment testing stations and Guangdong medicine packing product quality supervision and inspection offices. It is also responsible for the quality supervision and inspection in the state, provinces and districts, at the same time , it is the national compulsory CCC certification of products designated testing laboratory and inspection laboratory of CE authentication products authorized by Germany TUV PS
Medical Device Quality Management Committee, China Quality Association for Pharmaceuticals
Medical Device Quality Management Committee, China Quality Association for Pharmaceuticals is a commonweal social organization which is registered by Ministry of Civil Affairs. As the assistant of developing medical device quality management, it is a science and technology organization which is taken part in by people who focus on the management of medical device , as well as to help government contact with pharmaceutical enterprises. It is undertaken by China Quality Association for Pharmaceuticals and it is affiliated to Guangdong Medical Device Quality Supervision and Test Institute.
Osmunda Medical Device Consulting Organization
Osmunda Medical Device Consulting Organization which focuses on professional consulting in the field of medical device , founded in 2004, has set up seven wholly owned subsidiaries in Guangzhou, Beijing, Shanghai, Suzhou, Shenzhen, Jinan and America. We are able to provide fully solutions to medical device manufacturers, including marketing research, technical and capital services, workshop selection and design , clinical trail , quality system establishment , third party audit and global marketing approval.
The training certificate is issued solely by Guangdong Medical Device Quality Supervision and Test Institute, Medical Device Quality Management Committee, China Quality Association for Pharmaceuticals and Osmunda Medical Device Consulting Organization.
Eo Sterilization Confirm And Routine Control Training
For any questions and needs please contact us below
- Phone: 862062321333
- Address: 7th Floor, Jingui Business Building, No.982 Congyu, Guangzhou, China
- Website: http://www.osmundacn.net
Published date: November 28, 2012 -
- Business Description: Osmunda Medical Device Consulting Organization
(Guangzhou, Beijing, Shanghai, Suzhou, Shenzhen and Jinan) is the
largest and most professional consulting company in the field of medical
device in China. All Osmunda Consultant team members are from sizeable
medical devices enterprises, well known notified bodies and testing
organizations. We are well versed in global various medical device
quality system certification and product registration, such as SFDA
registration, QSR 820 system, FDA registration, ISO 13485 system, CE
certification etc. Our service includes clean room design, clinical
trail, third party audit, training of regulations and standards, etc.
Our headquarters is in Guangzhou, and we have five branch offices (Beijing, Shanghai, Suzhou, Shenzhen, Jinan) which could provide high speed local services and communication. By far, Osmunda has successfully assisted nearly 1,200 domestic and foreign enterprises in achieving various medical devices registration and certification. We will be your trustful partner and your most professional guide.
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