CHAPTER 4
Duties of Pharmacist
Section 33 A pharmacist in charge of the supervision of the production of psychotropic substances in Schedule III or Schedule IV shall;
(1)supervise the production in compliance with this Act;
(2)as certain the existence of labels and accompanying leaflets for psychotropic substances under Section 27(3);
(3)supervise the repacking and labeling of containers or packages in compliance with this Act;
(4)supervise the sale of psychotropic substances under Section 34;
(5)be in charge of supervision of the business all the time during working hours;
(6)do other acts as prescribed in the Ministerial Regulations.
Section 34 A Pharmacist in charge of the supervision of the sale of psychotropic substances in Schedule III or Schedule IV shall:
(1)supervise separate storage for psychotropic substances under Section 28 (2);
(2)supervise the execution under Section 28 (3);
(3)supervise the sale in compliance with this Act;
(4)supervise the preparation of psychotropic substances in accordance with the prescriptions of the persons referred to in (5);
(5)as certain the existence of labels on the containers or packages of psychotropic substances prepared in accordance with the prescriptions of medical practitioner, first-class practitioner in the branch of dentistry, or first-class veterinarian so as to be in compliance with the rules, procedure and conditions prescribed in the Ministerial Regulations;
(6)supervise the delivery of psychotropic substances in accordance with the prescriptions of the persons referred to in (5);
(7)supervise the keeping of record of acquisition and disposal of psychotropic substances in accordance with the rules, procedure and conditions prescribed in the Ministerial Regulations;
(8)ensure that psychotropic substance is not sold to a person without a prescription issued by the persons referred to in (5) or to a person without a license to produce, sell, or import psychotropic substances;
(9)be on duty of supervision of the business all the time during working hours;
(10)do other acts as prescribed in the Ministerial Regulations.
Section 35 A pharmacist in charge of the duty of supervision of the importation of psychotropic substances in Schedule III or Schedule IV shall:
(1)as certain that the imported psychotropic substances be in conformity with the formula of the registered preparation thereof;
(2)supervise the execution in connection with the labels and accompanying leaflets under Section 29 (3) and (4);
(3)supervise the sale of psychotropic substances under Section 34;
(4)be on duty of supervision of the business all the time during working hours;
(5)do other acts as prescribed in the Ministerial Regulations.
CHAPTER 5
Fake psychotropic substances, psychotropic substances
not being in conformity with standard and
deteriorated psychotropic substances
Section 36 A person shall not produce, sell or import psychotropic substances as follows:
(1)a fake psychotropic substance;
(2)a psychotropic substance which is not in conformity with its standard;
(3)a deteriorated psychotropic substance;
(4)a psychotropic substance which must be registered but has not been registered;
(5)a psychotropic substance the registration of preparation of which has been revoked by the Minister.
Section 37 The following psychotropic substances or articles shall be considered as fake psychotropic substances:
(1)an article which is totally or partly an imitation of a psychotropic substance;
(2)a psychotropic substance which shows the name of another psychotropic substance or the expiration date which is overstated;
(3)a psychotropic substance which shows a name or mark of its producer or the location of the place of production, which is false;
(4)a psychotropic substance which must be registered but has not been registered;
(5)a psychotropic substance which is produced not in conformity with the standard to such an extent that its active ingredient is less or more than ten percent of the minimum or maximum limit as prescribed in a Notification of the Minister under Section 6 (2) or as prescribed in the formula of the registered preparation.
Section 38 The following psychotropic substances shall be considered as psychotropic substances which are not in conformity with the standard:
(1)a psychotropic substance which is produced not in conformity with the standard to an extent that it is less or more than ten percent of the minimum or maximum limits as prescribed in a Notification of the Minister under Section 6 (2) or according to the formula of the registered preparation but not to the extent referred to under Section 37 (5);
(2)a psychotropic substance which is produced with the purity or any other characteristic, which is essential to its quality differing from the limits prescribed in a Notification of the Minister under Section 6 (2) or according to the formula of the registered preparation.
Section 39 The following psychotropic substances shall be deteriorated psychotropic substances:
(1)a psychotropic substance which has expired as shown on the label of the registered preparation;
(2)a psychotropic substance which has transformed so that it is the same as a fake psychotropic substance under Section 37 (5) or a psychotropic substance which is not in conformity with its standard under Section 38.
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