TEXT BOOK OF PHARMACEUTICAL QUALITY ASSURANCE
$9.08
Sale price
$9.08
Regular price
$9.08
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TEXT BOOK OF PHARMACEUTICAL QUALITY ASSURANCE
$9.08
Sale price
$9.08
Regular price
$9.08
Sold by Ergodemedia, an authorized reseller of Authentic New & Used Books with Free US Shipping.
30-day returns by mail · Refunded to original payment method | support@ergodemedia.com
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Returns & Refund
Returns accepted within 30 days of delivery. Returns are processed by mail. Refunds are issued to the original payment method within 5–7 business days of receiving the returned item.
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Return shipping at customer's expense · Book must be in the same condition as received · Refund to original payment method
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Safety & Compliance
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California Proposition 65 Warning
Some products sold on this website may expose you to chemicals known to the State of California to cause cancer, birth defects, or other reproductive harm.
www.P65Warnings.ca.gov
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Book Condition & Care Notice
Used books are graded and described accurately — condition details are listed on each product page. Books may contain previous owner's handwriting, highlights, or stamps unless stated as new. Store books away from direct sunlight and moisture to preserve their condition.
New books are sealed or unread. Used books are inspected before dispatch.
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Product Authenticity & Notice
All books sold by Ergodemedia are 100% authentic, sourced directly from publishers and trusted distributors. Book condition is accurately graded and described. Some books may contain previous owner's markings or inscriptions.
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Description
Quality assurance in the pharmaceutical industry encompasses rigorous standards and processes aimed at ensuring the safety, efficacy, and reliability of medicinal products. It involves implementing quality control measures, adhering to Good Manufacturing Practices (GMP), and embracing Total Quality Management (TQM) philosophies to foster continuous improvement. Regulatory guidelines, such as those outlined by the International Conference on Harmonization (ICH), play a pivotal role in standardizing practices and ensuring global alignment in quality standards. Moreover, initiatives like Quality by Design (QbD) emphasize proactive approaches to product development, emphasizing risk management and optimization throughout the manufacturing process. Adherence to international standards like ISO 9000 and ISO 14000, along with accreditation processes such as NABL, further solidify the commitment to quality excellence and regulatory compliance across all facets of pharmaceutical operations.
Product Notice
This book is sold in used condition unless explicitly stated as new.
Condition is graded and described accurately. Some books may contain
previous owner's markings, highlights, or inscriptions. This product
may contain chemicals known to the State of California to cause cancer
or reproductive harm. For more information visit
www.P65Warnings.ca.gov
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