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Modified-release Drug Delivery Technology
  • Language: en
  • Pages: 696

Modified-release Drug Delivery Technology

  • Type: Book
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  • Published: 2008
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  • Publisher: Unknown

None

Controlled Release Veterinary Drug Delivery
  • Language: en
  • Pages: 393

Controlled Release Veterinary Drug Delivery

  • Type: Book
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  • Published: 2000-07-20
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  • Publisher: Elsevier

Many controlled release veterinary drug delivery systems (CRVDDS) are presently in use, and recently there has been a host of new CRVDDS within veterinary medicine. The challenges of this area of drug delivery arise from the unique anatomy and physiology of the target animal, the cost constraints associated with the value of the animal being treated and the extended periods of time that delivery must be sustained for (often measured in months).The purpose of this book is to introduce the reader to the unique opportunities and challenges of the field of CRVDDS and to explain and discuss the basic controlled release principles underlying the development of CRVDDS. Its aim is to provide an over...

Preclinical Drug Development
  • Language: en
  • Pages: 374

Preclinical Drug Development

  • Type: Book
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  • Published: 2016-04-19
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  • Publisher: CRC Press

Preclinical Drug Development, Second Edition discusses the broad and complicated realm of preclinical drug development. Topics range from assessment of pharmacology and toxicology to industry trends and regulatory expectations to requirements that support clinical trials. Highlights of the Second Edition include: PharmacokineticsModeling and simula

The Pharmaceutical Regulatory Process
  • Language: en
  • Pages: 492

The Pharmaceutical Regulatory Process

  • Type: Book
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  • Published: 2008-12-02
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  • Publisher: CRC Press

This Second Edition examines the mechanisms and means to establish regulatory compliance for pharmaceutical products and company practices. It focuses on major legislative revisions that impact requirements for drug safety reviews, product regulatory approvals, and marketing practices. Written by top industry professionals, practicing attorneys, an

New Drug Approval Process
  • Language: en
  • Pages: 550

New Drug Approval Process

  • Type: Book
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  • Published: 2016-04-19
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  • Publisher: CRC Press

The thoroughly revised Fifth Edition of New Drug Approval Process supplies readers with the latest global changes that affect pharmaceutical product approval and influence how new products are researched and marketed.Updated chapters include:advances in international regulatory requirements, including ICH guidelines and harmonizationa step-by-step

Transdermal Drug Delivery Systems
  • Language: en
  • Pages: 296

Transdermal Drug Delivery Systems

  • Type: Book
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  • Published: 2002-10-29
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  • Publisher: CRC Press

Presents authoritative state-of-the-art discussions of the key issues pertinent to transdermal drug delivery, examining those topics necessary to enable a critical evaluation of a drug candidate's potential to be delivered across the skin; from physical chemistry and assessment of drug permeability to available enhancement technolgies, to regulator

Pharmaceutical Statistics
  • Language: en
  • Pages: 666

Pharmaceutical Statistics

  • Type: Book
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  • Published: 2009-12-23
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  • Publisher: CRC Press

Through the use of practical examples and solutions, Pharmaceutical Statistics: Practical and Clinical Applications, Fifth Edition provides the most complete and comprehensive guide to the various statistical applications and research issues in the pharmaceutical industry, particularly in clinical trials and bioequivalence studies.

Good Laboratory Practice Regulations
  • Language: en
  • Pages: 306

Good Laboratory Practice Regulations

  • Type: Book
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  • Published: 2007-01-19
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  • Publisher: CRC Press

Recent changes in the interpretation and enforcement of 21 CFR Part 11 have shifted the focus of Good Laboratory Practice (GLP) regulations to concentrate on the acceptance of electronic signatures, the archiving of data, the security of electronic documents, and the automation of laboratory procedures. This all-encompassing Fourth Edition addresse

The Smell of Football
  • Language: en

The Smell of Football

  • Type: Book
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  • Published: 2012
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  • Publisher: Unknown

None

Generic Drug Product Development
  • Language: en
  • Pages: 292

Generic Drug Product Development

  • Type: Book
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  • Published: 2016-04-19
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  • Publisher: CRC Press

Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence and bioequivalence for specialty drug products. It describes various scientific approaches and regulatory requirements for manufacturers who need to demonstrate the therapeutic equivalence of generic specialty dru