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Regulatory Links
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The pharmaceutical industry is a research-intensive industry. It has a continuous commitment to the discovery, development and marketing of new medicines. Overtime, the development of a new drug is becoming more complex, time consuming and costly.

For any new drug, the regulatory approval requires submission of scientific documents from pharmaceutical firms to substantiate the clinical safety and efficacy of the drug. For details of the requirements for regulatory approvals in different parts of the world, visit the following sites.

International   Hong Kong   New Zealand

www.ich.org
www.who.org

 

www.info.gov.hk/pharmser

  www.medsafe.govt.nz
Australia   Hungary   USA

www.health.gov.au/tga

  www.ogyi.hu   www.fda.gov
Canada   Japan    
www.hc-sc.gc.ca
 

www.nihs.go.jp

   
Europe   Latvia    

http://heads.medagencies.org/
http://www.emea.eu.int

 

www.vza.gov.lv

   

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