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13256988/09/01/2009 GE Healthcare URGENT MEDICAL DEVICE CORRECTION To: GE Ref: 86011 GE Healthcare IT 540 West Northwest Hwy Barrington, IL 60010 USA RE: GE Centricity? Laboratory; Software Version:
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86011custletterenglishdoc - mhra gov is a document required by the Medicines and Healthcare products Regulatory Agency (MHRA) in the United Kingdom. It is used for reporting certain information related to customer letters.
Any organization or individual that receives customer letters relating to medicines or healthcare products and operates within the regulatory jurisdiction of the MHRA is required to file 86011custletterenglishdoc - mhra gov.
To fill out 86011custletterenglishdoc - mhra gov, you need to provide the required information about the customer letters received. This may include details about the sender, the content of the letter, any potential adverse effects or complaints reported, and any actions taken by the recipient in response.
The purpose of 86011custletterenglishdoc - mhra gov is to ensure the reporting and documentation of customer letters related to medicines and healthcare products. It helps the MHRA monitor and assess the safety, quality, and effectiveness of these products.
The information that must be reported on 86011custletterenglishdoc - mhra gov may include details of the sender, date of receipt, content of the customer letter, any reported adverse effects or complaints, actions taken by the recipient, and any relevant follow-up information.
The specific deadline to file 86011custletterenglishdoc - mhra gov in 2023 has not been mentioned. Please refer to the official guidelines or contact the MHRA for accurate and up-to-date information regarding the filing deadline.
The penalty for the late filing of 86011custletterenglishdoc - mhra gov may vary depending on the regulations and policies of the MHRA. It is advisable to consult the official guidelines or contact the MHRA for detailed information regarding the penalties associated with late filing.
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