Being the teachers of Pharmaceutical Analysis and Quality Assurance for more than six year and 4 years at Teerthanker Mahaveer College of Pharmacy, Teerthanker Mahaveer University, Moradabad, India. We have developed passion for learning & writing more about the Regulations, like ICH, cGMP, ISO, USFDA, & other regulation. This creation of a book will help the pharmaceutical professionals in nourishing the knowledge of calibration of different equipment’s for developing a pharmaceutical industry quality control laboratory with optimized standards as well as in contract testing laboratory/institute. Keeping in view the calibration requirements for specific and highly accurate with precise analytical methods have been evolved with the passage of time which have now occupied pivotal and vital positions in most of the Official Compendia viz., USP, BP, Int.P., Eur. P, IP etc. The developments in the fields of pharmaceutical science and technology being utilized as on date, amalgamated with relatively stringent new regulations, namely: Federal Drug Authority (FDA); International Conference on Harmonization (ICH); Current Good Manufacturing Practices (cGMP); Pre-Approval Inspections.
"synopsis" may belong to another edition of this title.
I am Asst. Professor (Pharmaceutical Analysis and Quality Assurance) at Teerthanker Mahaveer College of Pharmacy, Teerthanker Mahaveer University, Moradabad, India. I had 6 year experience in pharmacy teaching as well as one year industrial exposure. I had published more than 13 national & international research publication.
"About this title" may belong to another edition of this title.
Shipping:
US$ 25.27
From Germany to U.S.A.
Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany
Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Being the teachers of Pharmaceutical Analysis and Quality Assurance for more than six year and 4 years at Teerthanker Mahaveer College of Pharmacy, Teerthanker Mahaveer University, Moradabad, India. We have developed passion for learning & writing more about the Regulations, like ICH, cGMP, ISO, USFDA, & other regulation. This creation of a book will help the pharmaceutical professionals in nourishing the knowledge of calibration of different equipment's for developing a pharmaceutical industry quality control laboratory with optimized standards as well as in contract testing laboratory/institute. Keeping in view the calibration requirements for specific and highly accurate with precise analytical methods have been evolved with the passage of time which have now occupied pivotal and vital positions in most of the Official Compendia viz., USP, BP, Int.P., Eur. P, IP etc. The developments in the fields of pharmaceutical science and technology being utilized as on date, amalgamated with relatively stringent new regulations, namely: Federal Drug Authority (FDA); International Conference on Harmonization (ICH); Current Good Manufacturing Practices (cGMP); Pre-Approval Inspections. 72 pp. Englisch. Seller Inventory # 9783659965463
Quantity: 2 available
Seller: AHA-BUCH GmbH, Einbeck, Germany
Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Being the teachers of Pharmaceutical Analysis and Quality Assurance for more than six year and 4 years at Teerthanker Mahaveer College of Pharmacy, Teerthanker Mahaveer University, Moradabad, India. We have developed passion for learning & writing more about the Regulations, like ICH, cGMP, ISO, USFDA, & other regulation. This creation of a book will help the pharmaceutical professionals in nourishing the knowledge of calibration of different equipment's for developing a pharmaceutical industry quality control laboratory with optimized standards as well as in contract testing laboratory/institute. Keeping in view the calibration requirements for specific and highly accurate with precise analytical methods have been evolved with the passage of time which have now occupied pivotal and vital positions in most of the Official Compendia viz., USP, BP, Int.P., Eur. P, IP etc. The developments in the fields of pharmaceutical science and technology being utilized as on date, amalgamated with relatively stringent new regulations, namely: Federal Drug Authority (FDA); International Conference on Harmonization (ICH); Current Good Manufacturing Practices (cGMP); Pre-Approval Inspections. Seller Inventory # 9783659965463
Quantity: 1 available
Seller: Revaluation Books, Exeter, United Kingdom
Paperback. Condition: Brand New. 72 pages. 8.66x5.91x0.17 inches. In Stock. Seller Inventory # 3659965464
Quantity: 1 available
Seller: moluna, Greven, Germany
Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Singh Bhuvnesh KumarI am Asst. Professor (Pharmaceutical Analysis and Quality Assurance) at Teerthanker Mahaveer College of Pharmacy, Teerthanker Mahaveer University, Moradabad, India. I had 6 year experience in pharmacy teaching as. Seller Inventory # 158125725
Quantity: Over 20 available