(Fox 2 Detroit) Detroit police opened an investigation last week after mummified remains were found in the garage of an occupied home. A would-be homebuyer made the shocking discovery Thursday, Fox 2 Detroit reported. medical interviewThe body was entombed in the backseat of a dust-covered Plymouth that was 25 or 26-years-old, the Detroit News reported. It appears the body had been there for years and was beyond the decomposition stage, the paper reported, citing a spokesman for the Wayne County Medical Examiners Office. The house had been rented to a family that never used the detached garage. A police spokesman told the paper the property owner told the family basically dont go in the garage, dont put anything in the garage. He said investigators would be contacting the property owner. It’s unclear to cops at this point who the dead person is or how he or she died and when. There may be answers when the autopsy is performed this week. The examination will include a Michigan University anthropologist, the News reported. Fox 2 also reported that police want to interview the property owner and to track down records that would show who lived in the house in the past and who registered the car. http://coachinglondonum9.bravesites.com/entries/general/helpful-tips-on-simple-solutions-for-consultantIn addition, the station reported, that the car was seized as evidence.
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This 2-day course provides the regulatory background and guides attendees through the complete equipment qualification, calibration and computer system validation processes from planning to reporting. It also helps to fully understand Part 11 and Annex 11 requirements to ensure and document integrity and other requirements for electronic records and signatures. Analytical equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex 11 requirements to ensure data integrity, security and availability. Recent EU and FDA inspection documents prove that qualification, validation and electronic laboratory are records are on target of inspectors. The large number of warning letters issued to laboratories also demonstrate that they struggle with either understanding or implementing the regulations. Learning Objectives: – Learn about the regulatory background and requirements for equipment qualification according to USP and computer system validation according to GAMP Guides – Be able to explain the difference between equipment calibration, qualification and system validation – Learn which equipment/systems need to be qualified or validated – Be able to allocate equipment and systems to USP and GAMP categories and to design and execute qualification/validation protocols accordingly – Understand the logic and principles of instrument qualification and system validation from planning to reporting – Be able to explain your company’s qualification and validation strategies – Understand how to archive raw data from hybrid systems: electronic vs. paper – Be able to define and demonstrate Part 11 compliance functionality to auditors and inspectors – Be able to develop inspection ready documentation during on-going routine operation – Learn how to ensure, document and audit integrity of raw data and other records For more information about this conference visit http://www.researchandmarkets.com/research/x2mmhp/analytical Contacts
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