Traditional Medicine Practice Act, 2000 (Act 575)
Section 15: (1) A certificate of a practitioner shall be cancelled by the Board on the recommendations of a
committee of the Board where the practitioner
(a) has been convicted of an offence under this Act or the Regulations,
(b) has breached any of the terms of the licence for the practice,
(c) has lost the qualification on the basis of which the registration was made,
(d) has been convicted to a term of imprisonment for a criminal offence, or
(e) has appeared before the Professional Standards and Ethics Committee which has
recommended the cancellation of the certificate.
(2) A certificate of a practitioner shall be cancelled if the Board considers it necessary in the interest
of public health.
Procedure to Follow
Registration
1. An application for the registration of Herbal medicinal product shall be made in writing.
2. An application form shall be completed in accordance with the sequence of appendices dated, signed and stamped by the applicant/license holder.
3. This shall be submitted in duplicate (hard and (or) soft copy) and accompanied by:
a. A covering letter addressed to the CEO of the Authority,
b. Samples of the product as specified in the Authority’s samples Schedule, packed in the final package ready for sale.
c. A non-refundable fee prescribed in the Authority’s approved fees Schedule.
Registration Variation
1. An application for the variation of registration of a product prior to re-registration shall be made to the Authority. This variation shall be approved by the Authority before any importation of the product shall be made into the country.
2. The application shall be accompanied by:
a. Supporting documentation for the variation.
b. Samples reflecting the variation as specified in the Authority’s samples Schedule.
c. Non-refundable variation fee as specified in Authority’s approved fees Schedule.
Re-Registration
1. An application for the re-registration of Herbal medicinal product should be made 3 (three) months before the expiration of the registration. 2. The application shall be accompanied by:
a. Supporting documentation for any changes since the product was last registered
b. Samples as specified in the Authority’s Sample Schedule.
c. A non-refundable application fee as specified in the Authority’s Fee Schedule....
Responsible Institution
No. 17 Indian Ocean Street, Nelson Mandela Avenue, Shiashie
- Email: fda@fda.gov.gh
- Website: https://www.fdaghana.gov.gh/
- GPS: GA-237-7316
- Telephone: (+233)302-233200/ 235100
Relevant Forms to Download
Not Available
Online System
Link Unavailable
Fees/ charges
Not Avaiable
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