VALIDATION IN PHARMACEUTICAL INDUSTRY

保存先:

書誌詳細
第一著者:	P.P.Sharma
フォーマット:	図書
言語:	英語
出版事項:	NEW DELHI VANDANA PUBLICATION 2022
版:	7th
主題:	QUALITY ASSURANCE
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

Text BooK of Pharmaceutical Validation
著者:: Sheetal Vikas Patil
出版事項: (2023)

Validation of Pharmaceutical Processes
著者:: Agalloco James
出版事項: (2020)

Textbook of Pharmaceutical Validation
著者:: SHeetal Vikas Patil
出版事項: (2023)

Textbook of Pharmaceutical Validation
著者:: A.A Kulkarni
出版事項: (2021)

Validated cleaning technologies for pharmaceutical manufacturing
著者:: LeBlanc, Destin A.
出版事項: (2019)

A TEXT BOOK OF PHARMACEUTICAL VALIDATION
著者:: Sheetal Patil
出版事項: (2021)

Perspectives of Different Validation and Calibration Techniques
著者:: Dr. Vishal D. Yadav
出版事項: (2023)

Concept of Quality Management in Pharmaceutical Industry
著者:: Potdar, Manohar A
出版事項: (2019)

PHARMACEUTICAL PROCESS VALIDATION: AN INTERNATIONAL VOL-129
著者:: Robert A Nash
出版事項: (2018)

PHARMACEUTICAL PROCESS VALIDATION: AN INTERNATIONAL VOL-130
著者:: Robert A.Nash
出版事項: (2018)

Good Manufacturing Of Pharmaceuticals
著者:: Graham.P.Bunn
出版事項: (2021)

Pharmaceutical Quality assurance and management
著者:: Bhusari, K.P
出版事項: (2021)

Pharmaceutical quality assurance
著者:: Potdar, Manohar A

Development and validation of analytical methods
著者:: ed. Riley, Christopher
出版事項: (2009)

Validation standard operating procedures : step by step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries
著者:: Haider, Syed Imtiaz

Equipment Qualification In The Pharmaceutical Industry
著者:: Ostrove Steven A
出版事項: (2023)

A Textbook of Molecular Pharmaceutics
著者:: Jhade, Deenanath
出版事項: (2022)

Text Book of Pharmaceutical Quality Assurance
著者:: Om Bagade
出版事項: (2022)

Pharmaceutical Quality Management & D.D.S.
著者:: Sopan Kumar Kar
出版事項: (2022)

Practical Approach in Quality Assurance in Pharmaceuticals
著者:: Vijay.R.Salunkhe
出版事項: (2021)

Pharmaceutical quality assurance for students of pharmacy
著者:: Potdar,Manohar A
出版事項: (2012)

Lab Manual Of Pharmaceutical Quality Assurance -II
著者:: Bhoomi.D.Patel
出版事項: (2020)

CGMP: Current good manufacturing practises for pharmaceuticals
著者:: Potdar ,Manohar A
出版事項: (2012)

validation and qualification in analytical laboratories : second edition
著者:: Huber, Ludwig

Development and Validation of Stability Indicating Method for Febuxostat
著者:: Mohanty Rahul

Development and Validation of Stability Indicating Method for Capecitabine
著者:: Agarwal Ayushi

Quality Assurance and Quality Management in Pharmaceutical Industry
著者:: Anjaneyulu, Y.
出版事項: (2021)

Quality Control of Packaging Materials in the Pharmaceutical Industry
著者:: Harburn, Kenneth
出版事項: (2008)

Good Manufacturing Practices for Pharmaceuticals
著者:: Graham P. Bunn
出版事項: (2019)

Drug Latentiation of a Gefitinib, An Epidermal Growth Factor Receptor (EGFR) Inhibitor, Anticancer (Pro-Drug of Gefitinib) with Cell Line Studies
著者:: Mrunal Sharma
出版事項: (2017)

Analytical Method Development and Validation of Dapagliflozin in Bulk by HPTLC and in Dosage Form by HPLC
著者:: Gupta Ankit

Pharmaceutical quality assurance
著者:: Potdar, Manohar A
出版事項: (2022)

Pharmaceutical quality assurance
著者:: Kashi, Anusuya
出版事項: (2022)

Pharmaceutical quality assurance
著者:: Potdar, Manohar A
出版事項: (2022)

Pharmaceutical Quality Assurance
著者:: "Dr. Manojkumar M. Nitalikar
出版事項: (2022)

Pharmaceutical quality assurance
著者:: Dahiya, Randhir Singh
出版事項: (2021)

Pharmaceutical Packaging Technology
著者:: Jain, U.K
出版事項: (2020)

Pharmaceutical Regulatory Process
著者:: Berry.Ira .R
出版事項: (2008)

Text Book of Drug Delivery System
著者:: Patil Prafull.P
出版事項: (2021)

Compliance auditing for pharmaceutical manufacturers
著者:: Ginsbury, Karen
出版事項: (2022)