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FOI – 2022-000077 Marketing And Communications team
Information request and response for FOI Reference: FOI – 2022-000077
MHRA Medical Device Safety Information – MDSI2309
MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture
National programme delivery
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Device Safety Information – DSI/2025/001
DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate
MHRA Device Safety Information – MDSI2306
MDSI2306 - NuVasive Specialized Orthopedics (NSO) PRECICE Titanium Systems: UK Suspension Lifted
Apply for tender opportunities
Use PCS-Tender to apply for a national healthcare tender. It's a secure eTendering system funded by the Scottish government.
Safety Information Message – SIM2501(U)
SIM2501(U) - Product Safety Report: MK Electric MK Essentials Electrical Three Pin Sockets with Switches: risk of burns
MHRA Medical Device Safety Information – MDSI2311U
MDSI2311U - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel: potential risk of infection - UPDATE
Understanding your payment reports
Find breakdowns of each predefined report type you'll receive via your ophthalmic monthly payment schedule.
Web and channel services
We understand web and can give you compliant, modern web sites and web apps fit for hosting evidence-based digital services.