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2. Equivalence studies for complex active ingredients and dosage forms. Bhattycharyya L; Dabbah R; Hauck W; Sheinin E; Yeoman L; Williams R AAPS J; 2005 Nov; 7(4):E786-812. PubMed ID: 16594632 [TBL] [Abstract][Full Text] [Related]
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5. Adopting a practical statistical approach for evaluating assay agreement in drug discovery. Sun D; Whitty A; Papadatos J; Newman M; Donnelly J; Bowes S; Josiah S J Biomol Screen; 2005 Aug; 10(5):508-16. PubMed ID: 16093560 [TBL] [Abstract][Full Text] [Related]
6. [Standardization as a basis planning and administration in drug industry and pharmacy (II)]. Wagler M Pharm Prax; 1970; 7():151-3. PubMed ID: 5469874 [No Abstract] [Full Text] [Related]
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9. Application of the equivalence test for analytical method transfers: testing precision using the United States Pharmacopoeia concept (1010). Schepers U; Wätzig H J Pharm Biomed Anal; 2006 Apr; 41(1):290-2. PubMed ID: 16338114 [TBL] [Abstract][Full Text] [Related]
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14. [General methods and specifications]. Anker L Ann Ist Super Sanita; 1975; 11(3-4):296-304. PubMed ID: 1234731 [TBL] [Abstract][Full Text] [Related]
15. Calibration of the Ph. Eur. Biological Reference Preparation (BRP) for tetanus vaccine (adsorbed) batch 3. Tierney R; Hockley J; Rigsby P; Terao E; Daas A; Buchheit KH; Sesardic D Pharmeur Bio Sci Notes; 2011 Jun; 2011(1):1-26. PubMed ID: 21619853 [TBL] [Abstract][Full Text] [Related]
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17. The U.S. Pharmacopeia's role in establishing public standards for aerosols. Srinivasan V J Aerosol Med; 1996 Mar; 9 Suppl 1():S13-7. PubMed ID: 10160053 [TBL] [Abstract][Full Text] [Related]
18. How good are our drugs? Miller LC Am J Hosp Pharm; 1970 May; 27(5):367-74. PubMed ID: 5422276 [No Abstract] [Full Text] [Related]
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