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Submitted by admin on Fri, 01/16/2009 - 15:22


Topics presented at GHWP Pre-Meeting Workshop held in conjunction with the 13th GHWP Meeting, 3-4 November 2008 in New Delhi, India

A Pre-Meeting Workshop was successfully held on 3-4 November 2008 in conjunction with the 13th GHWP Meeting. The workshop was organized as a platform for knowledge and experience sharing in various areas of medical device regulatory system.

Please download the presentations below.

Download file
AHWP_Role_of_Standards_Delhi_Nov_08_Gropp.pdf
China.ppt
Chinese_Taipei.ppt
Country_report_india.pdf
Hong_Kong_SAR.ppt
I_Future_of_MD_India_Vision_APitre.pdf
II_Opportunities_in_India_HBaid.pdf
III_Innovation_mfg_India_RVaidya.pdf
Indonesia.ppt
Philippines.ppt
Plenary_Benefits_o_Harmonization_CAlbertson.pdf
Plenary_Benefits_of_Harmonization_in_India_SRondeo.pdf
Singapore.ppt
Thailand.ppt
WorkshopI_MD_Regulations_RVBerberiam.pdf
WorkshopII_GEHC_Risk_Management_RVoelksen.pdf
WorkshopII_Risk_Mgmt_in_QS_Regulation_EKeith.pdf
WorkshopIII_Review_of_USFDA,_EU_and_SG5_Clinical_PKramsky.pdf
WorkshopIV_Conformity_Assessment_JWong.pdf
WorkshopV_ISO13485_JMoore.pdf
WorkshopV_Mfg_Operations_under_multiple_reg_requirements_JMcMahon.pdf
WorkshopVI_Natl_Comp_Authority_Reporting_Program_MLau.pdf
WorkshopVI_PMS_Regulation_in_India_SRondeo.pdf
WorkshopVI_Reporting_of_MD_Adverse_Even__PAuclair.pdf
WorkshopVII_Challenges_in_Regulatory_and_Compliance_CAlbertson.pdf
WorkshopVII_IVDD_DPierre.pdf

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