Request for production approval | Support administrative scrivener corporation

①Applicable to the terms of disqualification from petitioner (as a corporate body, official in charge) As a result, the applicant (as a legal entity, as an official in the development of an industry) shall be subject to any terms and conditions that may be inconsistent with the terms and conditions hereinafter, and may be obtained without law. Article 75 of the ``Japanese Medical Equipment Law'', Article 1, It is permissible to hang the item, and the person who is not yet 3 years old may be allowed to hang the item himself. b. Article 75 of the Japanese Medical Instruments Act, Article 2, ``Removal of items shall be noted, and the withdrawal shall be made by Nikki in its third year.'' c The person who was sentenced was not allowed to be sentenced or sentenced to be sentenced again, and his sentence was completed or suspended for three years. d Conflict Act, 《Poisonous and Harmful Substances Management Law》, 《Poisonous and Hazardous Substances Quality Control Law》, and other regulations.关药性法规或认证许多legal法规做的处处 (except for A to C), and self-contrary to date has not been published for many years. eAdults exposed to alcoholic beverages, cannabis, and alcoholic beverages. Persons who are responsible for the normal performance of laws and regulations of the Ministry of Health, Labor and Welfare, without any mental or physical residual disease. ② Persons responsible for production, production, production, medical equipment, quality control, post-market safety management, one person must be appointed. Medical equipment manufacturing Japanese industry qualification requirements Category 1 and 2 ① University or other equipment completed Physics, chemistry, biology, engineering (limited to mechanical engineering, electronic engineering, information science, metallurgy) In addition, the personnel in the field of education, medicine, medical science, and other medical engineering departments are subject to review, as well as medical equipment production, quality control, and post-production safety control. ②Completion of junior high school, high school or equivalent academic school Physics, chemistry, biology, engineering, biology, medicine, medical science or medical industry after completion of education Medical quality control system or post-production safety management cooperation work, or medical equipment production control system, quality control system or post-market safety control system cooperation work for as little as three years. ③ Approved by the Minister of Agriculture, Water, and Fisheries, who has the same qualifications as those who have previously worked in the same field or who have the same qualifications as those in high school. Category 3 ① Personnel who have completed junior high school, high school, or the equivalent or higher academic level under the old system of physics, chemistry, biology, engineering, education, medicine, medical science, or medical education. ② Completion of traditional junior high school, high school, or equivalent or above school education Physics, chemistry, biology, engineering, biology, medicine, medical education, additional medical supplies, non-medical supplies A team of people with less than three years of quality control and safety control after production in regenerative medicine, and medical equipment production control, quality control and safety control after production. ③ Approved by the Minister of Agriculture, Water, and Fisheries, who has the same qualifications as those who have previously worked in the same field or who have the same qualifications as those in high school. ③Manufacturer must appoint one person to ensure the quality of the product. Medical equipment manufacturing Japanese music industry qualification request category 1 ① must be submitted by the quality assurance department. ② Works related to personnel management, production control system, quality control system, and other similar operations have been carried out for as little as three years. ③Employees are required to have accurate, competent, and efficient work, as well as production control system, quality control system, and quantity control system. ④Normal operation of production control, quality control, mutual cooperation, and normal operations. Category 2, Category 3 ① Must be submitted to the Quality Assurance Department. ②Employees are required to have accurate, competent and efficient work, as well as production control system, quality control system and quantity control system. ③ Normal and efficient operation of production control, quality control, and cooperation between employees and non-members. ④ Person in charge of safety management: One person must be appointed.Required safety management personnel, security work after damage to medical equipment, production, and electricity. First category of medical equipment manufacturing and electronics industry qualification requirements: ① Must be paid by the safety control department. ② He has been working on security operations and other similar operations for only three years. ③Employees are required to be competent and to develop safety work in a timely manner. ④Proceed in a normal and harmonious manner with safety measures to prevent people from meeting. Category 2 and Category 3 ① Must be the person responsible for the safety control section. ②Employees are required to be competent and to develop safety work in a timely manner. ③Proceed in a normal and harmonious manner through safety measures to prevent people from meeting. ⑤ Required Establishment Basics (GQP System Ministerial Ordinance) and GVP Ministerial Ordinance (GVP Ministerial Ordinance). ■Concurrently responsible for production, safety management, quality assurance, and safety management. The first and second class of production, quality insurance, and safety management personnel are responsible for the quality insurance and safety management. The 3rd class can be used by the homeroom teacher at the same time. ■Three types of homeroom work at the same time in different types of production and medical fields (different types of medical equipment, books, etc.) A person responsible for the production of Japanese products, a person responsible for quality assurance, and a person responsible for safety management. ■Concurrently held the post of production engineering manager in Tokyo, at the same time as the company's production engineering department. * Availability varies by each prefecture. Medical equipment for medical use is available for admission. Support administrative register corporations, newly introduced medical equipment business enterprises, current manufacturers, production commerce, and Japanese machinery commerce. As we apply for advanced industrialization of medical equipment, this report covers a number of regional administrative agencies. We provide medical equipment, legal services, and legal services based on our work, administrative agents, and representative companies. I am an employee of the prefectures in Japan who own the prefectural government. If you would like more information, please contact us. We all have high expectations for this collaboration!

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a	Article 75 of Neji's Japanese Medical Equipment Law: 1. It is permissible to hang the item, and it is not permitted to hang it yourself.
b	Article 75 of the ``Japanese Medical Equipment Law'', Article 2, notes that the item must be withdrawn, and must be withdrawn by Nikki in its first three years.
c	The person who was sentenced was prohibited from being sentenced, and the sentence was not completed or the sentence was suspended for three years.
d	The Act on Conflict, the ``Poisonous and Harmful Substances Management Act'', the ``Poisonous and Harmful Substances Quality Control Act'', and other relevant laws and regulations (exceptions from A to C); Moreover, the self-rebellion has not started for more than two years.
e	Adults exposed to alcoholic beverages, cannabis, and alcoholic beverages.
f	Persons who are responsible for the normal implementation of laws and regulations of the Ministry of Health, Labor and Welfare without mental or physical residual disease.

Medical equipment manufacturing company	Qualification requirements
First category, second category	①	At university or elsewhere, physics, chemistry, biology, engineering (limited to mechanical engineering, electronic engineering, information science, metallurgy, etc.) and other examinations are required to confirm the quality control and production of medical equipment. After safety control, there are technical engineering departments) education, medicine, professional medicine, or medical personnel.
	②	Completion of junior high school, high school or equivalent school physics, chemistry, biology, engineering, geography, medicine, medical science, medical education, quality control of regenerative medicine, safety management after production. Work, medical equipment, production control, quality control, post-launch safety control, cooperating personnel with less than 3 years of experience.
	③	Approved by the Minister of Agriculture, Water, and Fisheries, and has the same level of staff as those who have previously worked in the department, or even in Kochi.
The third category	①	Persons who have completed junior high school, high school, or the equivalent or higher level of education under the old system, such as physics, chemistry, biology, engineering, pedagogy, medicine, medical science, or medical education.
	②	Completion of traditional junior high school, high school, or equivalent or above academic school physics, chemistry, biology, engineering, geography, medicine, medical science or medical education, quality control of non-medical products, non-medical products, and regenerative medicine. After production, safety control and control work, medical equipment production control, quality control, and safety control and control work after production are carried out by a staff of as little as three years.
	③	Approved by the Minister of Agriculture, Water, and Fisheries, and has the same level of staff as those who have previously worked in the department, or even in Kochi.

Medical equipment manufacturing company	Qualification requirements
the first sort	①	Please be sure to contact the Quality Assurance Department.
	②	It has been only three years since the personnel and production control system and quality control system and other similar operations have been carried out.
	③	Personnel must be qualified, competent, competent, productive, productive, quality, and competent.
	4	The normal operation of the production control system, the quality control system, and the mutual cooperation between employees and non-members.
2nd category, 3rd category	①	Please be sure to contact the Quality Assurance Department.
	②	Personnel must be qualified, competent, competent, productive, productive, quality, and competent.
	③	The normal operation of the production control system, the quality control system, and the mutual cooperation between employees and non-members.

Medical equipment manufacturing company	Qualification requirements
the first sort	①	Please be sure to contact the safety control department.
	②	I have been working on security operations and other similar operations for only three years.
	③	The personnel must be competent and work safely.
	4	A normal and harmonious process of safety work to prevent people from meeting.
2nd category, 3rd category	①	Please be sure to contact the safety control department.
	②	The personnel must be competent and work safely.
	③	A normal and harmonious process of safety work to prevent people from meeting.

First category, second category	A person responsible for production, quality assurance, and safety management who is also in charge of quality assurance and safety management.
The third category	Three types of work available to homeroom teachers.

Production Japanese song permission request

①Applicable to the terms of disqualification from petitioner (as a corporate body, official in charge)

②Person who purchased the product in production

③Product Quality Guarantee Seller

④ Person in charge of safety management

⑤Required enactment guidelines (GQP system ministerial ordinance) and GVP ministerial ordinance

Concurrently serves as production manager, quality assurance manager, and safety manager (three-person team)

Medical equipment for medical use is available for admission.