Testing Company Registration Testing Enterprise Registration

What is the registration process for housing construction testing qualifications?

1. First register a company with a registered capital of more than 6 million yuan in the Industrial and Commercial Bureau. 2. After the company is established, apply for the third-level general contracting qualification in the construction industry. According to the standard, 3 people need to be recruited. The above construction engineer (housing construction major) is registered with your company;

3. After the construction engineer is successfully registered, please prepare to submit the legal business license, organization code, capital verification report, articles of association, and office property rights Proof, ID cards, photos and professional title certificates of the legal person and the third chief engineer, ID cards and professional title certificates of more than 20 engineering and economic personnel, the roster of employees participating in the enterprise's pension insurance and payment invoices, and the list and invoices for purchasing related machinery and equipment. etc.;

4. After the above information is collected, download the application form from the Xinjiang Construction Information Network, and go to the local construction committee to apply for the purchase of qualification declaration code lock and record it;

5. Complete all documents in accordance with the requirements of the local construction committee, bring all original review documents, and submit them to the district construction committee for pre-review;

6. After the district construction committee completes the review within the statutory time, submit it to the municipal construction committee expert group for review and approval. , and then publicize and announce it online;

7. It is estimated that the qualification will be obtained within 3 months

Where should companies register for medical testing laboratories?

Anything related to medicine needs to be registered with the local medical administration to apply for registration.

In a company, which department should provide inspection standards, and which department should formulate inspection specifications?

Inspection standards involve the R&D department. The R&D department must verify the company's product inspection standards through tests and refer to relevant national testing standards, and report them to the relevant management departments for filing before they can be implemented.

Normally, the formulation of inspection specifications is made by the quality management department, and then reported to the relevant management department for filing. Only after obtaining the filing from the technical supervision department can it be determined as the company's inspection specifications.

How do foreign construction companies register when entering Kunming?

Article 7 of Yunnan Province's regulations on the management of enterprises from outside the province entering Yunnan to engage in construction activities. When enterprises from outside the province apply for registration in Yunnan, they should submit and present the originals and copies of the following materials at one time, and accept provincial housing and According to the information review organized by the Department of Urban and Rural Development, the Provincial Department of Housing and Urban-Rural Development can organize staff or entrust the local construction administrative department to conduct on-site inspection and verification of relevant matters according to the situation.

(1) Information required for registration by construction enterprises outside the province (Annex 1) (2) Information required for registration by supervision enterprises outside the province (Annex 2) (3) Information required for registration by inspection enterprises outside the province Information (Appendix 3) (4) Information required for registration by survey and design enterprises outside the province (Appendix 4) (5) Information required for registration by cost consulting enterprises outside the province (Appendix 5) (6) Information required for registration by bidding agencies outside the province Required information (Annex 6)

How to register medical testing items?

Medical device clinical trial filing procedures

1. Legal basis

1. "Regulations on the Supervision and Administration of Medical Devices" (State Council Order No. 650);< /p>

2. "Measures for the Registration and Management of In Vitro Diagnostic Reagents" (State Food and Drug Administration Order No. 5);

3. "State Food and Drug Administration's Regulations on the Clinical Use of Medical Devices" Announcement on Matters Related to Test Filing" (State Food and Drug Administration Announcement No. 87, 2015).

2. Application conditions

1. The applicant shall be a relevant unit or agent within the jurisdiction of Liaoning Province;

2. The applicant shall obtain a business license and Organization code certificate;

3. The clinical trial product has completed registration testing and the conclusion is qualified;

4. The clinical trial project has passed the ethical review and signed an agreement with the clinical trial institution or contract.

3. Application materials

1. "Medical Device Clinical Trial Registration Form" (see attachment) in duplicate;

2. Sponsor or agent Copy of business license;

3. Copy of ethics committee opinions;

4. Copy of clinical trial agreement or contract between the sponsor and clinical trial institution;

< p>5. Copy of medical device clinical trial approval document (third category medical devices that require clinical trial approval).

The above application materials should be true, complete, clear and neat; print them on A4 paper, make a cover and catalog, arrange them in the above order, and bind them into a volume; the copies should be clear and stamped with the official seal (multiple pages should be Stamped with a seam seal) and the original must be checked; the same items in the application materials should be filled in consistently.

4. Application procedures and time limits

1. Application. The sponsor submits medical device clinical trial filing materials to the Medical Device Registration Office of Liaoning Provincial Food and Drug Administration.

2. Review and filing. If the "Clinical Trial Registration Form" is completed and the submitted materials are complete and meet the formal requirements, it will be registered on the spot. The registration number will be filled in the "Clinical Trial Registration Form", stamped with a special registration seal, and a copy will be kept by the sponsor; if not If the application is filed, the sponsor shall be notified and the reasons shall be explained.

After the sponsor completes the clinical trial registration, if there is any change in the start and end dates of the trial project, it should notify the original registration management department within 10 working days after the change and keep a record of the information change.

5. Charges

Free.