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House leader calls for probe on DepEd s procurement of 39,000 laptops

House leader calls for probe on DepEd s procurement of 39,000 laptops
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ARTA to ease requirements for local COVID-19 vaccine makers

ARTA ARTA made the statement following President Duterte’s directive to set up a green lane for faster permit processing of local COVID-19 vaccine manufacturers to reduce dependency on imported jabs. In a statement, ARTA Deputy Director-General Ernesto Perez said one of the aims of the JMC that they are crafting is to standardize the documentary requirements, steps, and processing time for the applying companies during the pandemic. “We will implement those processes and permits under an emergency, without of course sacrificing the safety features of the COVID-19 vaccine we are envisioning to be manufactured in our own country,” he said.

FDA regulations need more flexibility in time of emergencies, Domingo admits

FDA regulations need more flexibility in time of emergencies, Domingo admits By ANNA FELICIA BAJO, GMA News Published April 22, 2021 1:09pm Food and Drug Administration (FDA) director general Dr. Eric Domingo on Thursday admitted that the agency needs more flexibility in implementing its regulations especially in time of emergencies. At a House Committee on Good Government and Public Accountability hearing, Domingo stressed that the FDA would support proposed measures in Congress that will give them flexibility during emergencies. Kailangan talaga ng FDA ng mas flexibility lalo na kung panahon ng emergencies at support the local pharmaceutical industry, Domingo said. (The FDA needs flexibility especially in times of emergencies as well as support the local pharmaceutical industry.)

Pharma industry cites red tape for over 1,500 of pending registration

BusinessWorld April 22, 2021 | 8:29 pm THE PHARMACEUTICAL sector called on the government to address the red tape in processing medicine registrations, citing more than 1,500 pending applications at the Food and Drug Administration (FDA) with some filed over seven years ago. In a House of Representatives panel hearing on Thursday, Philippine Chamber for Pharmaceutical Industries (PCPI) Technical Director Frances Evelyn P. Robles said the total is based on data from among its member companies. For certificates for product registrations that are low risk to no risk, there  are 479 pending applications since 2013. For high risk applications, Ms. Robles said 1,025 are pending based on data provided by 30 of its member companies.

House urges FDA to hasten procedures for CPR, EUA permits of local pharmaceuticals

House urges FDA to hasten procedures for CPR, EUA permits of local pharmaceuticals enablePagination: false endIndex: Metro Manila (CNN Philippines, April 18) House Speaker Lord Allan Velasco on Sunday appealed to the Food and Drug Administration to expedite the procedures concerning the application of local drug makers for certificates of product registration and emergency use authorization permits amid the pandemic. Velasco said local pharmaceuticals can boost the country’s response against COVID-19 but government agencies should strike a balance between the thorough study of drugs and making compliance easier for the drug firms. “There are countless reports of local drug manufacturers whose products have been stuck in regulatory limbo for years. These bureaucratic impediments are something that we need to eliminate, especially during a public health crisis,” he added.

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