Pharmaceutical

Pharmaceutical Drug Product Development and Process Optimization: Effective Use of Quality by Design

Pharmaceutical Drug Product Development and Process Optimization: Effective Use of Quality by Design by Sarwar Beg, Majed Al Robaian, Mahfoozur Rahman, Syed Sarim Imam, Nabil Alruwaili, Sunil Kumar Panda
2020 | ISBN: 1771888725 | English | 382 pages | PDF | 21.5 MB

Characterization of Pharmaceutical Nano- and Microsystems  eBooks & eLearning

Posted by arundhati at Oct. 31, 2020
Characterization of Pharmaceutical Nano- and Microsystems

Leena Peltonen, "Characterization of Pharmaceutical Nano- and Microsystems"
English | ISBN: 1119414040 | 2021 | 416 pages | PDF | 13 MB

Pharmaceutical Process Engineering and Scale-up Principles  eBooks & eLearning

Posted by AvaxGenius at July 5, 2023
Pharmaceutical Process Engineering and Scale-up Principles

Pharmaceutical Process Engineering and Scale-up Principles by Anil B. Jindal
English | PDF EPUB (True) | 2023 | 3031313798 | 18.5 MB

The book offers a comprehensive overview of the unit operations involved in the manufacturing process of solid and liquid dosage forms, along with the scale-up of each operation. This book is a valuable resource for professionals working in the pharmaceutical industry and researchers seeking to develop a comprehensive understanding of the various aspects of the manufacturing process.

Pharmaceutical Microbiology: Best Practices, Validation, Quality Assurance  eBooks & eLearning

Posted by Free butterfly at March 5, 2025
Pharmaceutical Microbiology: Best Practices, Validation, Quality Assurance

Pharmaceutical Microbiology: Best Practices, Validation, Quality Assurance by Michael Rieth
English | May 27, 2025 | ISBN: 3527354255 | 432 pages | PDF | 8.47 Mb
Natural Polymers for Pharmaceutical Applications: Volume 3: Animal-Derived Polymers

Natural Polymers for Pharmaceutical Applications: Volume 3: Animal-Derived Polymers by Amit Kumar Nayak, Md Saquib Hasnai, Dilipkumar Pal
2019 | ISBN: 1771888474 | English | 196 pages | PDF | 14 MB

Pharmaceutical Microbiology: Best Practices, Validation, Quality Assurance  eBooks & eLearning

Posted by Free butterfly at March 5, 2025
Pharmaceutical Microbiology: Best Practices, Validation, Quality Assurance

Pharmaceutical Microbiology: Best Practices, Validation, Quality Assurance by Michael Rieth
English | May 27, 2025 | ISBN: 3527354255 | 432 pages | PDF | 8.47 Mb

Pharmaceutical Regulatory Affairs  eBooks & eLearning

Posted by Free butterfly at April 4, 2025
Pharmaceutical Regulatory Affairs

Pharmaceutical Regulatory Affairs by Jigar Vyas, Nensi Raytthatha, Isha Shah
English | October 4, 2023 | 220 pages | ASIN: B0CKF4J2FX | PDF | 16 Mb

Risk-sharing in the Pharmaceutical Industry: The Case of Out-licensing  eBooks & eLearning

Posted by AvaxGenius at Feb. 17, 2023
Risk-sharing in the Pharmaceutical Industry: The Case of Out-licensing

Risk-sharing in the Pharmaceutical Industry: The Case of Out-licensing by Gerrit Reepmeyer
English | PDF(True) | 2006 | 306 Pages | ISBN : 3790816671 | 29.3 MB

The productivity in pharmaceutical research and development faces intense pres­ sure. R&D expenditures of the major US and European companies have topped US$ 33 billion in 2003 compared to around US$ 13 billion just a decade ago. At the same time, the number of new drug approvals has dropped from 53 in 1996 to only 35 in 2003. Moreover, the protraction of clinical trials has significantly reduced the effective time of patent protection. The consequences are devastating. Monopoly profits have started to decline and the average costs per new drug have reached a re­ cord level of close to US$ 1 billion today. As a result, any failure of a new sub­ stance in the R&D process can lead to considerable losses, and the risks of introduc­ ing a new drug to the market have grown tremendously. Particularly if a company is highly dependent on just a handful of mega-selling blockbuster drugs, the risks can be even greater. For example, Pfizer generated about 90% of its worldwide revenues in 2002 with just 8 products. Any shortfall of a promising late-stage drug candidate would have left Pfizer with a gaping hole in its product portfolio. In order to deal with these risks, many pharmaceutical companies have started to organize their R&D in partnership. In fact, more than 600 alliances in pharmaceutical R&D are signed every year.

Modern Aspects of Pharmaceutical Quality Assurance  eBooks & eLearning

Posted by hill0 at March 18, 2024
Modern Aspects of Pharmaceutical Quality Assurance

Modern Aspects of Pharmaceutical Quality Assurance:
Developing & Proposing Application models, SOPs, practical audit systems for Pharma Industry

English | 2024 | ISBN: 9819992702 | 531 Pages | PDF EPUB (True) | 36 MB

Pharmaceutical Nanobiotechnology for Targeted Therapy  eBooks & eLearning

Posted by AvaxGenius at Oct. 23, 2022
Pharmaceutical Nanobiotechnology for Targeted Therapy

Pharmaceutical Nanobiotechnology for Targeted Therapy by Hamed Barabadi, Ebrahim Mostafavi, Muthupandian Saravanan
English | PDF | 2022 | 641 Pages | ISBN : 3031126572 | 25.5 MB

The field of nanotechnology for targeted therapy initiated more than decade ago has grown fast and interest is increasing. Given the importance of the field for targeted drug and gene delivery systems, there are a large number of laboratory investigations today researching nanobiomaterials for diagnostic and therapeutic applications. Because of the ability of scientists to load nanoparticles with any agent, interest continues to grow and technology in this arena is rapidly evolving. These emerging nanobiomaterials-based medicines can overcome the disadvantages of traditional medicines by target-oriented and site-specific delivery of precise medicines (immunotherapeutic agents, chemotherapeutic agents, diagnostic agents, and so on).