A newsletter for those involved in clinical trials. Published 20 times a year by Canary Ltd

Japanese updates

The following articles on this topic have been published in CRAdvisor (CRA) – the year, issue number and starting page number for each are listed below:

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2005  
CRA 2005; 144:7 Japan will require third-party accreditation of low-risk devices.
CRA 2005; 152:3 How harmonised is SAE reporting to investigators?
   
2004  
CRA 2004; 126:6 Japanese drug makers look overseas for cheaper trials.
CRA 2004; 132:5 The EC-Japan MRA.
CRA 2004; 134:7 Trials to target female population in Japan.
CRA 2004; 134:7 Japan deregulates 350 drugs.
CRA 2004; 135:7 New system in Japan.
CRA 2004; 138:7 Japanese R&D taking shape.
   
2003  
CRA 2003; 103:8 EFPIA Japan.
CRA 2003; 104:6 SMOs facilitate drug development in Japan.
CRA 2003; 108:5 Japan's new medical regulatory institution.
CRA 2003; 109:6 Effects of genome-based medicine on Japanese medical regulation.
CRA 2003; 113:6 New law in Japan.
   
2002  
CRA 2002; 85:6 ICH 6 in Japan.
CRA 2002; 100:1 Brilliance and shadow brought to Japan by ICH.
   
2001  
CRA 2001; 66:3 Role of Head of Medical Institute in Japan.
CRA 2001; 69:6 Information access in Japan.
   
2000  
CRA 2000; 57:6 Dr Eitaka Tsuboi becomes President of WMA.
CRA 2000; 57:6 WMA adopts policy on communicable diseases in prisons.
CRA 2000; 57:6 New policy on organ and tissue transplantation.
   
1999  
CRA 1999; 28:6 Japan to accept foreign data.
CRA 1999; 32:6 ICH GCP complicates trials in Japan.
CRA 1999; 33:4 KIKOU advice for trials in Japan.
   
1998  
CRA 1998; 4:5 GCP compliance begins in Japan.

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