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Food And Drugs (Registration, Licensing And Inspection) Regulations
Cap. 291s04 · Revised Edition 2020 · 27 sections
- s. 1Citation
- s. 2Interpretation
- s. 3Prohibition of sale, etc. of unregistered drug
- s. 4Application for registration
- s. 5Orphan drugs
- s. 6Grant or refusal of product licence
- s. 7Application for amendment of product licence, upon change of circumstances
- s. 8Duration and renewal of product licence
- s. 9Labelling and packaging insert of drug
- s. 10Application for facility licence
- s. 11Grant of facility licence
- s. 12Duration and renewal of facility licence
- s. 13Non-transferability of facility licence
- s. 14Notification of changes
- s. 15Procedure on notification
- s. 16Procedure on change of the nature of business and change in ownership
- s. 17Display of facility licence
- s. 18Notification of closure of pharmaceutical facility
- s. 19Powers of competent authority
- s. 20Powers of inspectors
- s. 21Duties of inspectors
- s. 22Procedure on inspection
- s. 23Procedure on confiscation or destruction
- s. 24Application for re-inspection
- s. 25Revocation or cancellation of licence
- s. 26Application for review
- s. 27Transitional period