Intellectual Property Rights in Pharmaceutical Industry Theory and Practice. E-book. Formato EPUB Bayya Subba Rao   -  Bsp Books, 2019  - 

This book is aimed at pharmaceutical fraternity involving as students, researchers, teachers, regulators, policy makers to understand key aspects of intellectual property matters. The book is planned for quick understanding of basic concepts leading to practice in pharmaceutical Industry. The book provides clear cut understanding of national and international scenario of IPR matters. Salient Features of the Book: · Conventional English was used instead of legal language for the sake of initiators in learning IPR matters in pharmaceuticals. · Major emphasis is relating to pharmaceuticals. · History of IPR matters at global and national levels. · International Conventions on IPR matters only relating to pharmaceuticals · Introduction to every component of IPR with corresponding governing Acts, governing Ministry, and exclusivity periods with pharmaceutical related examples. · Objective and role of GATT, WTO and TRIPS agreement. · Introduction to The Patents Act, 1970 relating to inventions not patentable, types of patent applications, contents of a patent, patent office procedure timeline, PCT timeline, types of oppositions, types of infringement, expenditure incurred for filing and maintaining patents, rights of patentee, powers of controller of patents, compulsory licensing, and patent agents etc. · How to do literature search relating to non-patented and patented information for innovation and patent mining. · Comparison of principal The Patents Act, 1970 with three amendments. · Administration structure, protocol to become a member of WTO and procedure to resolve disputes. · Relationship of Drug Discovery, Drug regulatory and Market approval processes. · Various disputes settled at WTO of India relating to pharmaceuticals. · Judgments, case studies, notices relating to pre-grant opposition, post-grant opposition, compulsory licensing, infringements, working of patents, revoke of patents. · Possible questions at end of every chapter. · Above 100 frequently asked questions relating to Patents, Regulatory and Marketing relating to pharmaceuticals. · Statistics relating to patent grants at IPO, USPTO, and DMFs at USFDA relating to India.

Practical Pharmaceutical In-Organic Chemistry. E-book. Formato EPUB Bayya Subba Rao   -  Bsp Books, 2019  - 

The book is unique of its kind in giving clear understanding of the various experiments of pharmaceutical inorganic chemistry for undergraduate students. The experiments in the book are planned to suit all Indian Universities syllabi at the level of D. Pharm., B. Pharm., Post-Baccalaureate of Pharmacy and Pharm. D. The book is written considering all latest official standard procedures. Features Most important feature of the book is its self-explanatory presentation Special concentration is made on giving clear details of limit test for lead for easy understanding Every chemical reagent used in the experiment is explained for its purpose, a highlight in the book Experiments relating to assays were designed taking into consideration of all types of assays Identification tests of anions and cations were presented lucidly for easy memory by the students Semi-micro analysis is new for even teachers in some of the universities. A detailed lay out and necessary information is included A proper exposure of the student in handling viva-voce is necessary and all the possible questions are included Appended Features Additional Experiments Under every Category. Emphasized on specific test for purity of certain in-organic drugs. Complied list of Assay methods of small Molecule Drugs as per Indian Pharmacopoeia-2014.

Pharmaceutical Research Methodology and Bio-statistics Theory and Practice. E-book. Formato EPUB Bayya Subba Rao   -  Bsp Books, 2019  - 

“Pharmaceutical Research Methodology and Bio-Statistics: Theory and Practice” is aimed in understanding the fundamental concepts of developing a research bent of mind by careful planning, execution, collection of data and analyzing for statistical significance. The book is aimed at B. Pharm, Pharm D, Pharm D (PB), M. Pharm, allied course students, researchers at the academic and industry levels, Ph. D scholars, policy makers, regulators etc.