<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>119</id><JournalTitle>STUDY ON THE REGULATORY REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE IN COMMON WEALTH OF INDEPENDENT STATES</JournalTitle><Abstract>Dossier is a file document submitted based on the requirement of the drug approval process. It is a comprehensive
scientific document used to obtained worldwide licensing approval of a drug by diverse health authorities. There are different
requirements in different countries for registration of a product. Regulatory agencies require Pharmaceutical Dossiers to gain
approval to market drugs. Dossier is a document file which has technical and administrative information. Pharma companies
prepare dossier as per CTD / ASEAN CTD / non-CTD (country specific guideline).CIS countries follow their own country
specific dossier format.</Abstract><Email> praneebpharm@gmail.com</Email><articletype>Research</articletype><volume>4</volume><issue>8</issue><year>2014</year><keyword>CTD-Common Technical Document,ASEAN CTD, Non-CTD, CIS countries</keyword><AUTHORS>Praneetha K, Prakash B,Umasankar K,Alagusundaram M,Jayachandra Reddy P</AUTHORS><afflication>Krishna Teja Pharmacy College, Chadalawada Nagar, Tirupati - 517506, Andhra Pradesh, India.,Krishna Teja Pharmacy College, Chadalawada Nagar, Tirupati - 517506, Andhra Pradesh, India.,Krishna Teja Pharmacy College, Chadalawada Nagar, Tirupati - 517506, Andhra Pradesh, India.,Krishna Teja Pharmacy College, Chadalawada Nagar, Tirupati - 517506, Andhra Pradesh, India.,Krishna Teja Pharmacy College, Chadalawada Nagar, Tirupati - 517506, Andhra Pradesh, India.</afflication></Article></Articles>