1. First register a company with a registered capital of more than 6 million in the Industrial and Commercial Bureau.
2. After the company is established, it will apply for three-level general contracting qualification of construction industry. According to the standard, it is necessary to recruit more than 3 architects (majoring in building construction) to register with your company;
3. After successful registration, please prepare to submit the business license of legal person, organization code, capital verification report, articles of association of the enterprise, property right certificate of office space, ID cards, photos and professional title certificates of legal person and three chief engineers, ID cards and professional title certificates of more than 20 engineering economic personnel, employee roster and payment invoices for participating in endowment insurance, and lists and invoices for purchasing related machinery and equipment.
4. After the above data collection is completed, download the application form from Xinjiang Construction Engineering Information Online, and apply to the local Construction Committee to purchase the qualification declaration password lock and file it;
5. Complete all the documents according to the requirements of the local construction committee, bring all the original audit documents and submit them to the District Construction Committee for pre-examination;
6, the District Construction Committee in the statutory time after the review, reported to the Municipal Construction Committee expert group audit, qualified, and then online publicity, announcement;
7. The whole time is estimated to be qualified within 3 months.
Where does the enterprise handle the medical laboratory filing?
Anyone related to medicine needs to apply to the local medicine management department for filing.
In a company, which department should provide inspection standards and which department should formulate inspection specifications?
Inspection standards involve R&D departments, and our product inspection standards must be verified by R&D departments through experiments and with reference to relevant national inspection standards, and can only be implemented after being reported to relevant management departments for the record.
Generally speaking, the formulation of inspection specifications is made by the quality management department, and then reported to the relevant management departments for the record, and can only be determined as the company's inspection specifications after being filed by the technical supervision department.
How to record the entry of foreign construction enterprises into Kunming?
Provisions on the Administration of Construction Activities of Enterprises Outside Yunnan Province Article 7 Enterprises outside Yunnan Province shall submit and present the originals and photocopies of the following materials at one time for filing in Yunnan, and accept the data review organized by the Provincial Department of Housing and Urban-Rural Development, which may organize staff or entrust local construction administrative departments to conduct on-site investigation and verification of relevant matters according to the situation.
(1) Information required for filing of construction enterprises outside the province (attachment 1) (2) Information required for filing of supervision enterprises outside the province (attachment 2) (3) Information required for filing of testing enterprises outside the province (attachment 3) (4) Information required for filing of survey and design enterprises outside the province (attachment 4) (5) Information required for filing of cost consulting enterprises outside the province (attachment 5)
How to record medical laboratory items?
Application procedures for clinical trials of medical devices
I. Legal basis
1. Regulations on the Supervision and Administration of Medical Devices (Order No.650th of the State Council);
2. Measures for the Administration of Registration of in vitro Diagnostic Reagents (Order No.5 of China Food and Drug Administration);
3. Announcement of China Food and Drug Administration on Relevant Matters Concerning the Declaration of Clinical Trials of Medical Devices (Announcement No.87 of China Food and Drug Administration No.2015).
Second, the bidding conditions
1. The applicant is the relevant unit or agent within the jurisdiction of Liaoning Province;
2. The applicant shall obtain the business license and organization code certificate of the enterprise;
3 clinical trial products have been registered and tested and the conclusion is qualified;
4. The clinical trial project has passed the ethical review and signed an agreement or contract with the clinical trial institution.
Third, the application materials
1. medical device clinical trial record form (see annex) in duplicate;
2. A copy of the business license of the applicant or agent;
3. A copy of the opinions of the Ethics Committee;
4. A copy of the clinical trial agreement or contract between the applicant and the clinical trial institution;
Five copies of approval documents for clinical trials of medical devices (Category III medical devices that need to be approved for clinical trials).
The above application materials shall be true, complete, clear and tidy; Print on A4 paper, make cover and catalogue, arrange them in the above order, and bind them into a book; The copy should be clear and stamped with the official seal (multiple pages should be stamped with the riding seal) to check with the original; The same item in the application materials should be filled in the same way.
Four. Procedures and time limit for handling
1. The applicant shall submit the filing materials for clinical trials of medical devices to the Medical Device Registration Office of the US Food and Drug Administration in Liaoning.
2. Review and archiving. If the clinical trial filing form is complete, the submitted materials are complete and meet the formal requirements, it shall be filed on the spot, and the filing number shall be filled in the clinical trial filing form, stamped with the special seal for filing, and the applicant shall keep one copy; Not for the record, inform the applicant and explain the reasons.
After the applicant completes the clinical trial filing, if there is any change in the start and end date of the trial project, it should inform the original filing management department within 10 working days after the change, and keep the information change record.
Verb (abbreviation of verb) charging standard
It's free.