The main activities relating to the control of medicinal products include:

• Evaluation and approval of applications for new product licences, amendment and renewal of existing product licences, as well as the continual review of registered medicinal products.
• Evaluation and approval for import of unregistered medicinal products on a named patient basis.
• Approval for the import of medicinal products for the purpose of re-export.
• Evaluation and approval of applications for licences for the purpose of importation of registered medicinal products on a per consignment basis.
• Secretariat support for the Medicines Advisory Committee (MAC). 

• Guidelines

• Licences and Fees

• Target Processing Timelines

• Reclassified Medicines

• New Approvals

• FAQs on Medicinal Product Registration

• FAQs on Importation, Manufacturing and Retail

• FAQs on Bringing Personal Medication into Singapore