There is no requirement for a licensed pharmacist for Class II medical device companies,The following conditions must be met in order to start a Class II medical device manufacturing company:
(a) The person in charge of the enterprise shall have a college degree or above, or a junior or above title.
(B) the person in charge of the quality inspection organization should have college education or above, or intermediate or above title.
(C) the enterprise should occupy the corresponding proportion of the total number of employees above the junior title of engineering and technical personnel.
(d) the enterprise should have the appropriate product quality inspection capabilities.
(E) should be compatible with the production of products and scale of production, warehousing sites and environment.
(F) has the appropriate production equipment.
(vii) The enterprise shall collect and save the laws, regulations, rules and relevant technical standards related to the production and operation of the enterprise.
(viii) the production of sterile medical devices, should have a production site in line with the provisions.
In the provisional provisions of the licensed pharmacist qualifications of licensed pharmacists have been clearly defined:
(1) licensed pharmacists must abide by the professional ethics, faithful to their duties to the quality of medicines responsible for ensuring that the people's medicines are safe and effective as the basic guidelines.
(2) The licensed pharmacist must strictly implement the Drug Administration Law and the national regulations and policies on drug research, production, operation and use. The practicing pharmacist is responsible for advising, stopping, refusing to implement, and reporting to his or her superiors any behavior or decision that violates the Drug Administration Law and related regulations.
(3) The licensed pharmacist is responsible for the supervision and management of the quality of medicines within the scope of practice, and participates in the formulation and implementation of the total quality management of medicines, and handles the violation of the regulations in the unit.
Reference to the above: Baidu Encyclopedia - Class II Medical Devices