Literature DB >> 12033365

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.

Roger L Williams1, Wallace P Adams, Guirag Poochikian, Walter W Hauck.   

Abstract

This article reviews current and proposed approaches to content uniformity testing. In addition, the article proposes an approach that allows regulatory agencies and compendia to clearly state allowable consumer risk. Further, the article suggests that producers be allowed to control producer risk through selection of numbers of units and testing tiers. The approach facilitates risk communication to practitioners and patients/consumers, which is impeded with current approaches, and reduces regulatory and compendial burden.

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Year:  2002        PMID: 12033365     DOI: 10.1023/a:1015114821387

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  8 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

2.  Sample sizes for batch acceptance from single- and multistage designs using two-sided normal tolerance intervals with specified content.

Authors:  W W Hauck; R Shaikh
Journal:  J Biopharm Stat       Date:  2001-11       Impact factor: 1.051

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

Authors: 
Journal:  Fed Regist       Date:  2000-12-29

4.  Low first-spray drug content in albuterol metered-dose inhalers.

Authors:  T D Cyr; S J Graham; K Y Li; E G Lovering
Journal:  Pharm Res       Date:  1991-05       Impact factor: 4.200

5.  [Statistical considerations for weight variation and content uniformity tests].

Authors:  N Katori
Journal:  Eisei Shikenjo Hokoku       Date:  1994

6.  Optimal two-stage designs for phase II clinical trials.

Authors:  R Simon
Journal:  Control Clin Trials       Date:  1989-03

7.  Statistics: the problem of examining accumulating data more than once.

Authors:  K McPherson
Journal:  N Engl J Med       Date:  1974-02-28       Impact factor: 91.245

Review 8.  Sample size considerations for assessing individual bioequivalence based on the method of tolerance intervals.

Authors:  J D Esinhart; V M Chinchilli
Journal:  Int J Clin Pharmacol Ther       Date:  1994-01       Impact factor: 1.366

  8 in total
  3 in total

1.  Oral dosage form performance tests: new dissolution approaches.

Authors:  Walter W Hauck; Thomas Foster; Eric Sheinin; Todd Cecil; William Brown; Margareth Marques; Roger L Williams
Journal:  Pharm Res       Date:  2005-02       Impact factor: 4.200

2.  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

3.  Manipulation of Spray-Drying Conditions to Develop an Inhalable Ivermectin Dry Powder.

Authors:  Tushar Saha; Shubhra Sinha; Rhodri Harfoot; Miguel E Quiñones-Mateu; Shyamal C Das
Journal:  Pharmaceutics       Date:  2022-07-08       Impact factor: 6.525

  3 in total

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