මෙම අතුරුමුහුණත යන්ත්‍රයෙන් පරිවර්තනය කර ඇත. නීති සහ අධිකරණ තීන්දු ඒවායේ මූලාශ්‍ර භාෂාවෙන් පෙන්වනු ලැබේ.

පනවන ලද පරිදි

පටුන

National Medicines Regulatory Authority Act 2015 · පනවන ලද පරිදි · Part IV · General

62. Issuing of certificate of registration

නිල ඉංග්‍රීසි පරිවර්තනය. එය සිංහල හෝ දෙමළ පාඨයට වඩා වෙනස් නම් බලපවත්වන පාඨය කුමක්දැයි පනතේම සඳහන් වේ.

(1)

(a)

The Authority shall on registration of any medicine, issue a Certificate of Registration to the applicant who shall, hereinafter in this part of this Act, be referred to as “the holder of certificate”.

(b)

The Authority may grant full or provisional registration in respect of the medicine and the conditions for each type of registration shall be prescribed.

(c)

The period of registration granted shall be decided by the Authority as appropriate.

(2)

The Certificate of Registration shall include the purpose for which the registration is granted, its period of validity and the terms and conditions applicable thereto.

(3)

Upon obtaining the Certificate of Registration, the holder of certificate shall enter into an agreement with the

Authority to inform the Authority of any new developments of the medicine including the changes to indications, side effects, cautions, contra-indications, new recommendations by regulatory bodies in other countries, strictures, cancellations within a stipulated time period upon such facts and information being revealed.

s 63 සිට කියවන්න

Part V

General

Part V සිට කියවන්න

Part VI

Rules and Regulations

Part VI සිට කියවන්න

Part VII

Repeals and Transitional Provisions

Part VII සිට කියවන්න

Part VIII

Interpretation

Part VIII සිට කියවන්න