Medical Product Regulatory Affairs

Электронная книга
Добавлено 12.09.2020
Автор: Gary Walsh
Жанр: Научно-популярная литература
Год издания: 2019
Аннотация

Written in a clear and concise style by an experienced author, this attractively-priced book covers regulatory affairs in all major global markets for pharmaceuticals and medical devices, making it the most comprehensive in its field. Following a look at drug development, complete sections are devoted to national and EU regulatory issues, manufacturing license application and retention, and regulation in the USA. Other topics dealt with include CDER, CBER and marketing and manufacturing licenses, the ICH process and Good Laboratory/Clinical/Manufacturing Practices. Everything pharmacologists, bioengineers, pharma engineers, students in pharmacy and those working in the pharmaceutical industry need to know about medical regulatory affairs.

Полная версия

Отзывы о книге Medical Product Regulatory Affairs
Нет отзывов
Добавить отзыв

Чтобы добавить отзыв Вам нужно зарегистрироваться или авторизироваться

Новости
Библиотека
Обратная связь
Поиск