Literature DB >> 12356095

International Conference on Harmonisation; guidance on Q6A specifications: test procedures and acceptance criteria for new drug substances and new drug products: chemical substances. Notice.

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Abstract

The Food and Drug Administration (FDA) is publishing a guidance entitled "Q6A Specifications: Test Procedures and Acceptance Criteria for New Drug Substances and New Drug Products: Chemical Substances." The guidance was prepared under the auspices of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The guidance describes or provides recommendations concerning the selection of test procedures and the setting and justification of acceptance criteria for new chemical drug substances and new drug products produced from them. The guidance is intended to assist in the establishment of a single set of global specifications for new drug substances and new drug products.

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Year:  2000        PMID: 12356095

Source DB:  PubMed          Journal:  Fed Regist        ISSN: 0097-6326


  40 in total

1.  Where are we now and where do we go next in terms of the scientific basis for regulation on bioavailability and bioequivalence? FDA Biopharmaceutics Coordinating Committee.

Authors:  R L Williams; W Adams; M L Chen; D Hare; A Hussain; L Lesko; R Patnaik; V Shah
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2000 Jan-Mar       Impact factor: 2.441

Review 2.  Content uniformity and dose uniformity: current approaches, statistical analyses, and presentation of an alternative approach, with special reference to oral inhalation and nasal drug products.

Authors:  Roger L Williams; Wallace P Adams; Guirag Poochikian; Walter W Hauck
Journal:  Pharm Res       Date:  2002-04       Impact factor: 4.200

3.  Nonclinical dose formulation analysis method validation and sample analysis.

Authors:  Monica Lee Whitmire; Peter Bryan; Teresa R Henry; John Holbrook; Paul Lehmann; Thomas Mollitor; Susan Ohorodnik; David Reed; Holly D Wietgrefe
Journal:  AAPS J       Date:  2010-08-14       Impact factor: 4.009

Review 4.  Statistical thinking and knowledge management for quality-driven design and manufacturing in pharmaceuticals.

Authors:  Evdokia Korakianiti; Dimitrios Rekkas
Journal:  Pharm Res       Date:  2010-12-14       Impact factor: 4.200

5.  Investigation of the multi-step dehydration reaction of theophylline monohydrate using 2-dimensional powder X-ray diffractometry.

Authors:  Cletus Nunes; Arumugam Mahendrasingam; Raj Suryanarayanan
Journal:  Pharm Res       Date:  2006-09-01       Impact factor: 4.200

6.  Quantification of crystallinity in substantially amorphous materials by synchrotron X-ray powder diffractometry.

Authors:  Cletus Nunes; Arumugam Mahendrasingam; Raj Suryanarayanan
Journal:  Pharm Res       Date:  2005-08-31       Impact factor: 4.200

7.  An investigation into the importance of "very rapid dissolution" criteria for drug bioequivalence demonstration using gastrointestinal simulation technology.

Authors:  Ivan Kovacevi; Jelena Parojci; Marija Tubi-Grozdanis; Peter Langguth
Journal:  AAPS J       Date:  2009-05-20       Impact factor: 4.009

8.  Disintegration of highly soluble immediate release tablets: a surrogate for dissolution.

Authors:  Abhay Gupta; Robert L Hunt; Rakhi B Shah; Vilayat A Sayeed; Mansoor A Khan
Journal:  AAPS PharmSciTech       Date:  2009-04-23       Impact factor: 3.246

Review 9.  The science of USP 1 and 2 dissolution: present challenges and future relevance.

Authors:  Vivian Gray; Gregg Kelly; Min Xia; Chris Butler; Saji Thomas; Stephen Mayock
Journal:  Pharm Res       Date:  2009-01-23       Impact factor: 4.200

10.  Study of the applicabilty of content uniformity and dissolution variation test on ropinirole hydrochloride tablets.

Authors:  Edina Vranić; Alija Uzunović
Journal:  Bosn J Basic Med Sci       Date:  2008-05       Impact factor: 3.363

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