METHOD DEVELOPMENT BY RP-HPLC, DISSOLUTION TESTING, MICROBIOLOGICAL QUALITY TEST AND ITS VALIDATION FOR AN ANTI- HYPERTEN

保存先:

書誌詳細
第一著者:	MODI SHAILE
フォーマット:	図書
出版事項:
主題:
タグ:	タグ追加タグなし, このレコードへの初めてのタグを付けませんか!

類似資料

ASSAY AND DISSOLUTION METHOD DEVELOPMENT AND VALIDATION OF THE ANTIPSYCHOTIC DRUG BY RP-HPLC
著者:: LUND KAPIL

ANALYTICAL METHOD DEVELOPMENT AND VALIDATION OF DISSOLUTION METHOD OF AN ANTI-MALARIAL DRUG BY HPLC
著者:: SHAH TRISHLA

METHOD DEVELOPMENT AND VALIDATION FOR DISSOLUTION, ASSAY AND RS FOR DRUG X TABLET BY RP-HPLC
著者:: MEHTA SAVAN

STABILITY INDICATING ANALYTICAL METHOD DEVELOPMENT, DISSOLUTION, ASSAY AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS
著者:: BORSE SIDDHARTH

METHOD DEVELOPMENT AND VALIDATION FOR ASSAY TEST OF SUSTAINE RELEASE PELLETS OF LEVOSULPRIDE BY RP-HPLC
著者:: NAYAK SURESH

DEVELOPMENT AND VALIDATION OF ANALYTICAL METHOD FOR ASSAY OF AN ANTI MIGRAINE DRUG BY RP-HPLC
著者:: BHATT AARTI

DEVELOPMENT AND VALIDATION OF ASSAY METHOD OF AN ANTI- HYPERLIPEDIMIC DRUG BY USING RP-HPLC
著者:: UPADHYAY NEELAM

Pharmaceutical Dissolution Testing
著者:: Banakar, Umesh V.
出版事項: (2017)

Pharmaceutical dissolution testing
著者:: Dressman,Jennifer
出版事項: (2005)

Pharmaceutical dissolution testing
著者:: Banakar,Umesh V
出版事項: (2010)

PHAEMACEUTICAL DISSOLUTION TESTING
著者:: BANAKAR UMESH V [A]
出版事項: (1992)

PHARMACEUTICAL DISSOLUTION TESTING
著者:: DRESSMAN JENNIFER B [E], KRAMER JOHANNES [E]
出版事項: (2005)

PHARMACEUTICAL DISSOLUTION TESTING
著者:: DRESSMAN JENNIFER B [E], KRAMER JOHANNES [E]
出版事項: (2007)

PHARMACEUTICAL DISSOLUTION TESTING
著者:: BANAKAR UMESH V
出版事項: (1993)

PHARMACEUTICAL DISSOLUTION TESTING
著者:: DRESSMAN,JENNIFER
出版事項: (2007)

PHARMACEUTICAL DISSOLUTION TESTING
著者:: BANAKAR UMESH V
出版事項: (1992)

Pharmaceutical dissolution testing
著者:: Banakar, Umesh V.
出版事項: (2010)

Pharmaceutical dissolution testing
著者:: Banakar, Umesh V.
出版事項: (2023)

METHOD DEVELOPMENT AND VALIDATION FOR DISSOLUTION TEST OF THE TABLET CONTAINING QUETIAPINE
著者:: AWASTHI YOGESH

METHOD DEVELOPMENT FOR DETERMINATION OF ASSAY, RELATED SUBSTANCES AND DISSOLUTION OF AN ANTI-ANGINAL DRUG BY RP- HPLC
著者:: GOYAL KANIKA

"Method Development and Validation for Dissolution of Ezetimibe in 10 mg dosage form Using RP-HPLC method"
著者:: Vidhi Kiran Shah
出版事項: (2018)

DEVELOPMENT ANAD VALIDATION OF STABILITY INDICATING RP-HPLC METHOD FOR DETERMINATION OF ANTI - PARKINSONISM DRUG AND ITS
著者:: SHAH DOLITA

DEVELOPMENT AND VALIDATION OF ANALYTICAL METHOD FOR RELATED SUBSTANCES OF AN ANTI-TUBERCULOSIS DRUG BY RP-HPLC
著者:: JOSHI ANANDKUMAR

ANALYTICAL METHOD DEV. AND VALIDATION OF STABILITY INDICATING RP-HPLC METHOD FOR ESTIMATION OF ASSAY AND DISSOLUTION OF DRUG A& B IN ANTI DI
著者:: NUPUR KETAN GOR

DEVELOPMENT OF STABILITY INDICATING ASSAY METHOD AND ITS VALIDATION OF ETOMIDATE INJECTION BY RP - HPLC
著者:: BRAHME PRASHANT

DEVELOPMENT OF STABILITY INDICATING METHOD FOR ASSAY OF THE ADENOSINE INJECTION BY RP-HPLC AN ITS VALIDATION
著者:: NATEKAR RAJAS

DEVELOPMENT AND VALIDATION OF RELATED SUBSTANCES METHOD FOR QUANTITATIVE ESTIMATION OF AN ANTI-MIGRAINE DRUG BY RP-HPLC
著者:: LOKARE LEENA

DEVELOPMENT AND VALIDATION OF ASSAY AND RELATED SUBSTANCES METHOD OF AN ANTI-DIABETIC DRUG BY USING RP-HPLC
著者:: SEHGAL RAVINDER

ASSAY METHOD DEVELOPMENT AND VALIDATION OF ANTI- HYPERTENSIVE DRUGS IN TABLET DOSAGE FORM BY RP-HPLC METHOD
著者:: MAHIDA VIRAJSINH

A RP-HPLC METHOD DEVELOLPMENT AND VALIDATION FOR ANTIHYPERTENSIVE FORMULATION
著者:: SHROFF KUSHAL

METHOD DEVELOPMENT AND VALIDATION OF DULOXETINE HYDROCHLORIDE SR PELLETS BY RP-HPLC
著者:: CHAVAN DHANANJAY

METHOD DEVELOPMENT AND VALIDATION FOR ESTIMATION OF TOLPERSONE HYDROCHLORIDE IN TABLET BY RP-HPLC
著者:: AGARWAL SNEHA

METHOD DEVELOPMENT AND VALIDATION FOR ESTIMATION OF METRONIDAZOLE IN TABLETS BY USING RP-HPLC
著者:: BHATT RUSHABH

DEVELOPMENT AND VALIDATION OF ANALYTICAL METHOD FOR ASSAY OF AN ANTIBACTERIAL DRUG BY RP-HPLC
著者:: VERMA SAROJ DWARIKA PRASAD

METHOD DEVELOPMENT AND METHOD VALIDATION FOR AN ENTERIC COATED TABLET USING RP-HPLC
著者:: CHAUHAN JYOTI

ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR DISSOLUTION TEST OF FORMULATION CONTAINING VALSARTAN - AN ANTIHYPERTENS
著者:: HIRAY ARTI

ANALYTICAL METHOD VALIDATION OF AN ANTI-VIRAL FORMULATION BY HPLC
著者:: KUMARI SUDESH

DEVELOPMENT OF RP-HPLC METHOD FOR CHROMATOGRAPHIC PURITY OF ANTI-RETROVIRAL DRUG LAMIVUDINE
著者:: KAKKAR SALONI

METHOD DEVEOPMENT AND MEHTOD VALIDATION OF DELAYED RELEASE CAPSULE 'A' FOR THE TEST OF DISSOLUTION
著者:: JINAK K.PATEL
出版事項: (2019)

STABILITY INDICATING ASSAY METHOD DEVELOPMENT AND VALIDATION OF DOXERCALCIFEROL INJECTION BY RP-HPLC
著者:: ABAK ANUPAM