To draft and revise good practices for drug research, manufacturing, distribution and use, and supervise their implementation | The SFDA allots 35 working days as its official timeframe for reviewing applications; however, actual review times are often longer, particularly if additional information is requested |
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Issue Date: 2015 Scope: Decument Type : Microbiology of food and animal feeding stuffs -- Horizontal method for the detection of potentially enteropathogenic Vibrio spp | By clicking the triangle to the left of the year, you may also filter by quarter, month, or day within a given year |
Do we need an in-country representative in Saudi Arabia? Nonetheless, the Ministry of Health retains its other main functions-regulatory development and oversight, healthcare resource allocation, and medical research and education.
24Title to the Content of this site vests with the Copyright holder | In July 1999, as part of medical insurance reform, SFDA released its first list of over-the-counter OTC medications, and in 2000, the state began to regulate OTC and prescription drugs separately |
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By clicking the triangle to the left of the year, you may also filter by quarter, month, or day within a given year | To authorise and organise high-standard continuing professional development programmes for fund directors and upgrade training for potential directors |
The Dashboard Legend below explains the information presented in the dashboard in further detail: Dashboard Legend Court No | The SFDA […] Membership Ordinary Membership in SFDA includes individuals and firms providing directorships to the Fund Management and Asset Management community, those would primarily be including Independent Non-Executive Directors INED Associate Membership in SFDA includes top firms and financial institutions providing fund administration services, custodians, auditors, compliance firms, technology providers, legal firms, asset management firms, private banks, and trust companies, to name a few |
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In fact, SFDA required all pharmaceutical companies in China to obtain GMP certificates from SFDA by June 30, 2004 to be licensed to sell their drug products in China | , extreme heat , Declaration of Compliance to Saudi regulations, and attestation of electrical compatibility for active devices Emergo helps with medical device approvals in Saudi Arabia Emergo is an international consulting firm that works exclusively for medical device and IVD companies |