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Special Lecture on Clean Workshop for Final Sterilization Medical Device Production | Online Training | Jinnan Testing

Special Lecture on Clean Workshop for Final Sterilization Medical Device Production | Online Training | Jinnan Testing

  • Time of issue:2022-09-02
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Special Lecture on Clean Workshop for Final Sterilization Medical Device Production | Online Training | Jinnan Testing

Special Lecture on Clean Factory for Final Sterilization Medical Device Production | Online Training
September 23, 2022


Dear customer
Thank you and your team for their long-term support of Jinnan Medical Testing business!
The design, construction, acceptance, standardized management, and daily monitoring of clean room factories play a crucial role in the quality control, quality management, and product risk management of enterprise production. Medical device manufacturing enterprises can improve the management quality of clean workshops and ensure the production environment of products by understanding the relevant legal and regulatory requirements for the construction and acceptance of clean workshops, as well as the problems that are prone to occur during clean workshop testing.
In order to further improve the standardized management ability of medical device enterprises in the production of clean workshops, we are holding an online sharing meeting related to the "Final Sterilization Medical Device Production Clean Workshop Special Explanation". We sincerely invite you to participate!
The specific meeting arrangements are as follows:
1、 Conference organization
Shenzhen Jinnan Medical Testing Technology Co., Ltd
Shunwei Environmental Technology (Shenzhen) Co., Ltd
Shenzhen Jinpai Medical Packaging and Sterilization Service Co., Ltd
Dongguan Security Medical Packaging Technology Co., Ltd
2、 Meeting time
September 23, 2022, 14:00-17:00
3、 Meeting format
Online live streaming
4、 Meeting content

time Content

14:00-15:30

1) Environmental selection and environmental parameter design requirements for production areas
2) Process design and architectural design
3) Air purification
4) Acceptance requirements after construction completion
5) Maintenance and upkeep of clean workshop

15:30-17:00

1) Introduction to Domestic and Foreign Standards for Clean Room Testing
2) Clean room pollution sources
3) Clean room environmental control
4) Clean room daily monitoring

5、 Conference presenters
Teacher Liu
I majored in clinical medicine and have been engaged in the establishment of quality systems and process validation in the pharmaceutical industry for many years;
Proficient in the design and maintenance of clean workshops related to sterile medical devices, as well as the validation and confirmation of medical device production processes;
Proficient in all pharmaceutical industry related standards such as ISO13485, GB50457, YY0033, and on-site inspection guidelines for medical device production quality management standards;
I am currently serving as the Technical Manager of Shunwei Environmental Technology (Shenzhen) Co., Ltd.
Teacher Zhang
Master of Microbiology
Engaged in inspection and laboratory management related to medical devices for many years;
Proficient in microbial testing and cleanroom testing related to sterile medical devices;
Proficient in all international and domestic standards related to testing, such as GB, ISO, etc;
Proficient in quality control and evaluation criteria for sterile medical devices;
I am currently serving as the laboratory manager of Shenzhen Jinnan Medical Testing Technology Co., Ltd.
6、 Attendees
Enterprise technical research and development personnel, inspection personnel.
7、 Contact registration method
1. Training contact person: Mr. Zheng/Jinnan Testing and Marketing Department
2. Registration phone number: 19129490661/13923648758 (same WeChat account)
3. Registration email: ks09@kingservice-ps.com
4. Registration method:

 

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