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Pharmaceutical Vendors Approval Manual - A Comprehensive Quality Manual for API and Packaging Material Approval
Erfan Syed Asif
Taylor & Francis Ltd (2021)
Kovakantinen kirja
120,70
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ostoskoriin kpl
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Basics of Pharmaceutical Manufacturing and Quality Operations - A Comprehensive Guide
Erfan Syed Asif; Shahid Bader Usmani
Taylor & Francis Ltd (2024)
Kovakantinen kirja
132,40
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ostoskoriin kpl
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Pharmaceutical Vendors Approval Manual - A Comprehensive Quality Manual for API and Packaging Material Approval
Erfan Syed Asif
Taylor & Francis Ltd (2024)
Pehmeäkantinen kirja
65,60
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ostoskoriin kpl
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Quality Operations Procedures for Pharmaceutical, API, and Biotechnology
Syed Imtiaz Haider; Erfan Syed Asif
Taylor & Francis Inc (2012)
Kovakantinen kirja
118,40
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ostoskoriin kpl
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Quality Control Training Manual - Comprehensive Training Guide for API, Finished Pharmaceutical and Biotechnologies Laboratories
Syed Imtiaz Haider; Syed Erfan Asif
Taylor & Francis Inc (2011)
Kovakantinen kirja
207,90
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Quality Control Training Manual - Comprehensive Training Guide for API, Finished Pharmaceutical and Biotechnologies Laboratories
Syed Imtiaz Haider; Syed Erfan Asif
Taylor & Francis Ltd (2018)
Pehmeäkantinen kirja
73,00
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ostoskoriin kpl
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Pharmaceutical Vendors Approval Manual - A Comprehensive Quality Manual for API and Packaging Material Approval
120,70 €
Taylor & Francis Ltd
Sivumäärä: 152 sivua
Asu: Kovakantinen kirja
Julkaisuvuosi: 2021, 13.12.2021 (lisätietoa)
Kieli: Englanti
This book provides stepwise guidance on how to evaluate, audit, qualify and approve an active pharmaceutical ingredient (API) and packaging material manufacturer and supplier to enhance the GMP within the industry. The book will also be beneficial for institutions conducting pharmaceutical technology courses in terms of GMP and GLP applications. The Pharmaceutical Vendors Approval Manual provides readers and front-line health care products manufacturers, R&D management and biotech laboratories all the information they need to know to develop a GMP-oriented industry with trained and skilled personnel and manufacture products that meet GMP and regulatory requirements. This book provides a simple, concise and easy to use reference tool covering basic quality concepts and the elements of vendor’s assessment, qualification and approval required by the pharmaceutical educational institutions and professional certification bodies. It is equally relevant to Quality Assurance officers, Quality Control Analysts, Quality Auditors and other personnel involved in GMP/GLP services in the company. The book will also be beneficial for the institutions conducting Pharmaceutical technology study courses in terms of GMP and GLP applications.

This book






provides readers and front-line health care products manufacturers, R&D management and biotech laboratories all the information they need to know to develop a GMP-oriented industry with trained and skilled personnel and manufacture products that meet GMP and regulatory requirements



covers basic quality concepts and the elements of vendor’s assessment, qualification and approval required by the pharmaceutical educational institutions and professional certification bodies



provides stepwise guidance on how to evaluate, audit, qualify and approve an API and packaging material manufacturer and supplier to enhance the GMP within the industry



provides ready to use regulatory documentation, e.g. letter of commitment, questionnaire, SOP, etc. required for API and Packaging Materials contract

Provided material can be easily tailored to incorporate changes to add in-house vendor’s qualification requirements.

Erfan Syed Asif, Ph.D is a Senior Consultant at PharmEng Technology.

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Pharmaceutical Vendors Approval Manual - A Comprehensive Quality Manual for API and Packaging Material Approvalzoom
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ISBN:
9781032030883
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