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Serie: Drugs and the pharmaceutical sciences
GebondenEngels9780367024673
17-3-2020
The over-riding premise for biotechnology in this book is bringing novel products to market to substantially advance patient care and disease mitigation. Meer
GebondenEngels9780367538002
30-8-2024
This volume presents pharmaceutical research through theoretical concepts, methodologies and ethical issues. It fulfils publication ethics course work requirements for students. Meer
PaperbackEngels9780367447748
2-12-2019
This useful reference describes the statistical planning and design of pharmaceutical experiments, covering all stages in the development process-including preformulation, formulation, process study and optimization, scale-up, and robust process and formulation development. Meer
PaperbackEngels9780367712150
9-10-2024
Continuous manufacturing of pharmaceuticals, including aspects of modern process development is highlighted in this book with both the ‘why’ and the ‘how’, emphasizing process modeling and process analytical technologies. Meer
PaperbackEngels9780367783778
31-3-2021
Compaction of powder constituents—both active ingredient and excipients—is examined to ensure consistent and reproducible disintegration and dispersion profiles. Meer
PaperbackEngels9780367779764
31-3-2021
This book continues to be the definitive reference on drug metabolism with an emphasis on new scientific and regulatory developments. It has been updated based on developments that have occurred in the last 5 years, with new chapters on large molecules disposition, stereo-selectivity in drug metabolism, drug transporters and metabolic activation of drugs. Meer
PaperbackEngels9780367735081
18-12-2020
The first edition of Pharmaceutical Extrusion Technology, published in 2003, was deemed the seminal book on pharmaceutical extrusion. Now it is expanded and improved, just like the usage of extrusion has expanded, improved and evolved into an accepted manufacturing technology to continuously mix active pharmaceutical ingredients with excipients for a myriad of traditional and novel dosage forms. Meer
PaperbackEngels9780367741457
29-1-2024
This fully revised edition covers the rapid advances in the science of agglomeration, process control, process modelling, scale-up, emerging particle engineering technologies, along with current regulatory changes presented by some of the prominent scientist and subject matter experts around the globe. Meer
PaperbackEngels9780367736873
18-12-2020
Aqueous-based film coating has become routine in the pharmaceutical industry. This process eliminates the use of organic solvents and thus avoids economic, environmental, and toxicological issues related to residual solvents and solvent recovery. Meer
GebondenEngels9780367707668
1-3-2023
Discusses scientific solutions and process analytical technology to enable continuous manufacturing in the development of new drugs.
Includes short stories about how some companies have adopted CM and what their drivers were and what benefits were realized. Meer
PaperbackEngels9780367497026
13-12-2021
The over-riding premise for biotechnology in this book is bringing novel products to market to substantially advance patient care and disease mitigation. Meer
PaperbackEngels9780367400590
19-6-2019
This up-to-the-minute Second Edition of an incomparable resource describes in detail the bases for developing dosage forms for use in animals-highlighting the data necessary to meet regulatory approval. Meer
PaperbackEngels9780367451882
2-12-2019
This book examines the sequence of events and methodology in the industrial clinical research process; a reference for multidisciplinary personnel. It is the conceptual framework involving the philosophical, economic, political, historical, regulatory, planning, and marketing aspects of the process. Meer
GebondenEngels9780367334772
12-5-2021
This fully revised edition of Handbook of Pharmaceutical Granulation Technology covers the rapid advances in the science of agglomeration, process control, process modelling, scale-up, emerging particle engineering technologies, along with current regulatory changes presented by some of the prominent scientist and subject matter experts around the globe. Meer
GebondenEngels9780367336271
13-12-2022
The GLP regulations have been enacted since 1978 and are currently under a proposed FDA amendment to revise terminology and accommodate other changes relating to advances in technology related to the industry. Meer
PaperbackEngels9780367402013
5-9-2019
This volume provides a single-source of reviews for all the important colloidal drug delivery systems, including nanoparticles, liposomes, niosomes, microemulsions and ointments. Meer
PaperbackEngels9780367402914
19-6-2019
A comprehensive treatment of the science, technology, and regulation of rate-controlled administration of therapeutic agents, with coverage of the basic concepts, fundamental principles, biomedical rationales, and potential applications. Meer
PaperbackEngels9780367385057
10-10-2019
Addressing the increased use of protein and peptide candidates as treatments for previously untreatable diseases, this comprehensive and progressive source provides the reader with a roadmap to an increased understanding of issues critical for successfully developing a protein or peptide therapeutic candidate. Meer
PaperbackEngels9780367552497
30-6-2020
When a biological drug patent expires, alternative biosimilar products are developed. The development of biosimilar products is complicated and involves numerous considerations and steps. Meer
GebondenEngels9780849375835
19-1-2007
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. Meer