10 March 2021 – All Trade Regulatory Government Agencies (TRGAs) are now mandated to get on board with the TradeNet, an interoperable online platform to reduce processing time and harmonize the permitting procedures involved in import and export, per the Anti-Red Tape Authority (ARTA)’s recently issued memorandum circular. The memorandum circular issued by ARTA last.. read more
CBP Phase 1 launched, to improve Philippines’ Starting a Business performance in Doing Business report
28 January 2021 – Earlier today, the Anti-Red Tape Authority (ARTA), Department of Information and Communications Technology (DICT), Securities and Exchange Commission, Bureau of Internal Revenue, Social Security System, Philippine Health Insurance Corporation, Pag-IBIG Fund, Food and Drug Administration, and eighteen pilot Local Government Units (LGUs) launched the first phase of the Central Business Portal.. read more
ARTA inspects Valenzuela and Caloocan BOSS, inks MOU for ARTA package
13 January 2021 – With the recently concluded inspection of the business one-stop shops or BOSS of Valenzuela City and Caloocan City today, the Anti-Red Tape Authority (ARTA) had already inspected nine out of the 17 local government units (LGUs) in Metro Manila. As with its previous inspections, the ARTA team checked on the important.. read more
ARTA to LGUs: Implement Business One-Stop Shops
1 January 2021 – The Anti-Red Tape Authority (ARTA) is calling on all Local Government Units (LGUs) to fully implement their Business One-Stop Shops (BOSS) for this year’s business registration and business license renewals. Starting this January, ARTA shall be conducting a series of on-the-spot inspections on LGUs in the National Capital Region and other.. read more
ARTA calls on FDA to streamline registration process of vaccines and medical supplies
5 January 2021 – The Anti-Red Tape Authority (ARTA) is calling on the Food and Drug Administration (FDA) to ensure that the process for the Certificate of Product Registration (CPR) for all vaccines and other medical supplies will be streamlined and shall not be subjected to unnecessary processes and requirements. The FDA previously submitted to.. read more