Order Total (1 Item Items):
Shipping Destination:
Asif Erfan Syed (77 results)
Skip to main search results
Search filters
Product Type
- All Product Types
- Books (77)
- Magazines & Periodicals (No further results match this refinement)
- Comics (No further results match this refinement)
- Sheet Music (No further results match this refinement)
- Art, Prints & Posters (No further results match this refinement)
- Photographs (No further results match this refinement)
- Maps (No further results match this refinement)
- Manuscripts & Paper Collectibles (No further results match this refinement)
Condition Learn more
- New (69)
- As New, Fine or Near Fine (8)
- Very Good or Good (No further results match this refinement)
- Fair or Poor (No further results match this refinement)
- As Described (No further results match this refinement)
Binding
Collectible Attributes
- First Edition (No further results match this refinement)
- Signed (No further results match this refinement)
- Dust Jacket (No further results match this refinement)
- Seller-Supplied Images (20)
- Not Print on Demand (53)
Language (1)
Free Shipping
Seller Location
Seller Rating
-
Quality Operations Procedures for Pharmaceutical, API and Biotechnology
Published by Taylor & Francis Group, 2012
ISBN 10: 1439886903 ISBN 13: 9781439886908
Language: English
Condition: New. pp. 584 1st Edition.
-
-
Condition: New. First edition Includes bibliographical references and index.
-
Condition: New.
-
Quality Control Training Manual
Published by Taylor & Francis Group, 2011
ISBN 10: 1439849943 ISBN 13: 9781439849941
Language: English
Condition: New. pp. 484.
-
Condition: As New. Unread book in perfect condition.
-
Condition: As New. Unread book in perfect condition.
-
-
-
Pharmaceutical Vendors Approval Manual
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
Condition: New. In.
-
Pharmaceutical Vendors Approval Manual: A Comprehensive Quality Manual for API and Packaging Material Approval
Published by Taylor & Francis Ltd, 2022
ISBN 10: 1032038136 ISBN 13: 9781032038131
Language: English
Seller: THE SAINT BOOKSTORE, Southport, United Kingdom
Seller rating 5 out of 5 stars
Paperback / softback. Condition: New. New copy - Usually dispatched within 4 working days. 310.
-
Pharmaceutical Vendors Approval Manual : A Comprehensive Quality Manual for Api and Packaging Material Approval
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: New.
-
-
Quality Control Training Manual: Comprehensive Training Guide for API, Finished Pharmaceutical and Biotechnologies Laboratories
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
Condition: New. In.
-
Quality Control Training Manual : Comprehensive Training Guide for Api, Finished Pharmaceutical and Biotechnologies Laboratories
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: New.
-
Pharmaceutical Vendors Approval Manual : A Comprehensive Quality Manual for Api and Packaging Material Approval
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: As New. Unread book in perfect condition.
-
-
Pharmaceutical Vendors Approval Manual: A Comprehensive Quality Manual for API and Packaging Material Approval
Published by CRC Press 2021-12-13, 2021
ISBN 10: 1032030887 ISBN 13: 9781032030883
Language: English
Hardcover. Condition: New.
-
Brand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.
-
Quality Control Training Manual : Comprehensive Training Guide for Api, Finished Pharmaceutical and Biotechnologies Laboratories
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: As New. Unread book in perfect condition.
-
Condition: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
-
Condition: New. Brand New Original US Edition. Customer service! Satisfaction Guaranteed.
-
-
Condition: New.
-
Brand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.
-
Condition: New. 1st edition NO-PA16APR2015-KAP.
-
Pharmaceutical Vendors Approval Manual (Paperback)
Published by Taylor & Francis Ltd, London, 2024
ISBN 10: 1032038136 ISBN 13: 9781032038131
Language: English
Paperback. Condition: new. Paperback. 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 vendors 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 vendors 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 vendors qualification requirements.Erfan Syed Asif, Ph.D is a Senior Consultant at PharmEng Technology. 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. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
-
Paperback. Condition: Brand New. reprint edition. 484 pages. 9.01x5.98x1.06 inches. In Stock.
-
Condition: New.
-
Condition: New.
