Lachman/Lieberman's The Theory And Practice Of Industrial Pharmacy
- Publisher: MEDICAL BOOKS
- Availability: In Stock
- SKU: 37516
- Number of Pages: 1203
Rs.650.00
Rs.750.00
Tags: 2024 , 2024 Edition , 2024 latest Edition , 2024-2025 , advanced drug delivery technologies. , controlled release , drug excipients , drug production , drug stability testing , EMA , FDA , GMP , good manufacturing practices , industrial pharmacy , Industrial Pharmacy 2024 , Lachman Lieberman , Lachman/Lieberman's , large-scale production , Latest Edition , liposomal formulations , liquid dosage forms , modern industrial pharmacy , nanoparticles , pharmaceutical automation , pharmaceutical dosage forms , pharmaceutical manufacturing , pharmaceutical packaging , pharmaceutical packaging materials , pharmaceutical professionals , pharmaceutical students , preformulation , regulatory compliance , Review 2024-2025 , Roop K. Khar , S.P. Vyas , solid dosage forms , sterile products , sustained release , transdermal drug delivery , WHO
This comprehensive textbook is a go-to reference in the field of pharmaceutical sciences, focusing on industrial pharmacy. It covers various aspects of drug formulation, manufacturing processes, quality control, and the industrial production of pharmaceuticals. This book bridges theoretical knowledge with practical application, making it invaluable for students, professionals, and researchers in pharmaceutical technology and drug manufacturing. The 4th edition of this widely acclaimed textbook has been updated with the latest technological advancements and regulatory practices in the pharmaceutical industry.
Key Points:
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Fundamentals of Pharmaceutical Dosage Forms:
- Detailed discussion of the principles and processes behind the formulation of solid, liquid, and semi-solid dosage forms.
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Drug Formulation and Preformulation:
- Introduction to preformulation studies to evaluate drug properties such as solubility, stability, and compatibility with excipients.
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Pharmaceutical Manufacturing Processes:
- Examination of drug manufacturing processes, with a focus on large-scale production, processing, and industrial techniques.
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Controlled and Sustained Release Drug Delivery:
- Insight into controlled and sustained release formulations to improve therapeutic outcomes and patient compliance.
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Pharmaceutical Quality Control:
- Exploration of the principles and methods of quality control and quality assurance in industrial settings, ensuring compliance with regulatory standards.
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Regulatory Affairs and GMP:
- Coverage of Good Manufacturing Practices (GMP) and regulatory requirements from the FDA, EMA, and WHO, crucial for pharmaceutical production.
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Sterile Product Development:
- Detailed overview of the formulation, production, and testing of sterile dosage forms, including injectables and ophthalmic products.
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Pharmaceutical Packaging and Stability Testing:
- A comprehensive look at packaging technologies and stability testing to ensure drug safety, protection, and extended shelf life.
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Advances in Drug Delivery Systems:
- Examination of innovative drug delivery systems, such as transdermal patches, nanoparticles, and liposomal formulations.
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Industrial Pharmacy Practices:
- Practical insights into industrial-scale production, automation, and the application of pharmaceutical technologies in modern industrial pharmacy.
Conclusion:
Lachman/Lieberman's The Theory and Practice of Industrial Pharmacy is an essential resource for students, researchers, and professionals engaged in the pharmaceutical industry. The textbook covers the entire spectrum of industrial pharmacy, from drug development and formulation to large-scale production, quality control, and regulatory compliance. Updated with the latest technologies and global standards, it provides a comprehensive guide for understanding and applying industrial pharmaceutical principles.
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Writer ✤ Roop K. Khar (Author), S.P. Vyas (Author)