Handbook of Pharmaceutical Manufacturing Formulations - Over-the-Counter Products (Volume 5 of 6)

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Introduction to "Handbook of Pharmaceutical Manufacturing Formulations - Over-the-Counter Products (Volume 5 of 6)"

The pharmaceutical industry remains one of the most dynamic and complex fields, and the demand for accessible knowledge on formulation development continues to grow. "Handbook of Pharmaceutical Manufacturing Formulations - Over-the-Counter Products (Volume 5 of 6)", written by Sarfaraz K. Niazi, serves as a comprehensive reference guide for professionals, students, and enthusiasts in the pharmaceutical and healthcare sectors focused on non-prescription products. With an emphasis on practical formulation strategies for over-the-counter (OTC) medications, this book bridges the gap between pharmaceutical science and real-world manufacturing.

Detailed Summary of the Book

This volume is part of the critically acclaimed Handbook of Pharmaceutical Manufacturing Formulations series, which covers a broad spectrum of drug formulation approaches. Specifically, Volume 5 is dedicated to OTC pharmaceutical products, which encompass a wide range of formulations intended for self-administration without requiring a prescription. These products include analgesics, antacids, antihistamines, topical creams, dietary supplements, cold and flu remedies, and more.

The book provides a meticulous breakdown of ingredient selections and formulation techniques suitable for global markets, recognizing the differences in regulations and healthcare practices across regions. It assists in mastering the intricacies of scaling up laboratory-developed formulations into cost-effective manufacturing processes. Each formulation includes detailed information about active and excipient ingredients, preparation procedures, and quality control considerations, ensuring the production of safe, effective, and high-quality products.

Whether addressing solubility issues, pH adjustments, or stability challenges, this volume explains critical processes with simple language and practical case examples. With a strong regulatory perspective, the book takes into account compliance with agencies like the FDA, EMA, and WHO. Additionally, it examines the varying stability and shelf-life requirements for over-the-counter products, making it easier for manufacturers to meet consumer expectations within a regulated framework.

Key Takeaways

  • Comprehensive instructions for OTC product formulation, including liquid, solid, and semi-solid dosage forms.
  • Insights into global regulatory compliance, including labeling requirements, quality standards, and market variations.
  • Guidance on identifying the appropriate excipients to enhance product stability, effectiveness, and patient acceptability.
  • Practical advice on manufacturing scale-up techniques and troubleshooting formulation issues.
  • Detailed considerations for packaging, shelf-life, and stability testing specific to OTC products.

Famous Quotes from the Book

"The responsibility of manufacturing an over-the-counter product does not end with placing it on a store shelf; it extends to anticipating how consumers will integrate it into their healthcare routine."

"Formulation science is not just about mixing chemicals; it is about creating solutions that integrate efficacy, stability, and consumer trust into a unified product."

"In the dynamic realm of OTC products, success is defined by the delicate balance between accessibility, compliance, and innovation."

Why This Book Matters

Over-the-counter products, while often underestimated, play an essential role in public health by empowering individuals to take charge of their own well-being. This book is a vital resource for pharmaceutical professionals striving to meet the growing demand for safe and efficient self-medication solutions. By offering an exhaustive guide to formulations and manufacturing processes, it ensures that quality OTC products reach consumers worldwide.

Furthermore, in an industry characterized by ever-evolving regulations and consumer demands, having a comprehensive resource such as this is invaluable. It not only boosts the confidence of those involved in drug formulation but also ensures a deeper understanding of the science and art of pharmaceutical compounding.

This book is particularly relevant to formulators, manufacturers, regulators, and students who strive to stay ahead in the fiercely competitive over-the-counter product market. Its focus on practical applications, coupled with a strong scientific foundation, makes it a must-have guide for anyone seeking to elevate their expertise in pharmaceutical manufacturing.

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