Search: "Drug development" Filter:"Drug development"

7 tagged events, 2 books found.


Tagged events

September 2019

SEP 4
Biocore extends a warm welcome to the distinguished speakers, delegates, researchers, and pharmaceutical professionals, ...

Dubai,
United Arab Emirates

SEP 4
Biocore extends a warm welcome to the distinguished speakers, delegates, researchers, and pharmaceutical professionals, ...

Dubai,,
United Arab Emirates

October 2019

OCT 24
Over 350 delegates representing global pharmaceutical organisations, leading biotechnology companies, and internationall...

London,
United Kingdom

November 2019

NOV 7
20th Pharmacovigilance 2019 07th November 2019, Kohinoor Continental Hotel, Mumbai, India 20th Pharmacovigilance 20...

Mumbai,Maharashtra,
India

May 2020

MAY 26
Join over 400 leaders, experts and scientists at the renowned R&D Series, helping to shape the future of drug discovery ...

Berlin,
Germany

September 2020

SEP 7
Pharmaceutical development is a costly and time-consuming process. A science-led, risk-based approach can save time and ...

November 2020

NOV 17
The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole...

Books

The Generic Challenge

Understanding Patents, FDA and Pharmaceutical Life-Cycle Management (Sixth Edition)

by Martin A. Voet

04/13/2020

This Sixth Edition of The Generic Challenge provides important new updates on current regulatory, legal and commercial issues affecting brand and generic pharmaceutical products, including new laws establishing generics for biologics, and changes brought about by the recently enacted America Invents Act. It explains clearly and understandably the roles of patents, FDA regulation of drugs and the Hatch Waxman Act in commercial drug development in light of generic challenges and how improvements in innovative drug products provide benefits to patients while extending the commercial lives of the drugs. There is simply no other book of its kind on this important subject. REVIEWS [W]ho would benefit from a book toeing the line of enabling appreciation without going into too much detail? .... ...

The Generic Challenge

Understanding Patents, FDA and Pharmaceutical Life-Cycle Management (Fifth Edition)

by Martin A. Voet

09/07/2016

This Fifth Edition of The Generic Challenge provides important new updates on current regulatory, legal and commercial issues affecting brand and generic pharmaceutical products, including new laws establishing generics for biologics, and changes brought about by the recently enacted America Invents Act. It explains clearly and understandably the roles of patents, FDA regulation of drugs and the Hatch Waxman Act in commercial drug development in light of generic challenges and how improvements in innovative drug products provide benefits to patients while extending the commercial lives of the drugs. There is simply no other book of its kind on this important subject. REVIEWS [W]ho would benefit from a book toeing the line of enabling appreciation without going into too much detail? .... ...