EU Regulatory Affairs Made Easy: The express line to rock-solid competence in European pharmaceutical regulatory affairs

At last! The single most cost- and time-effective introduction to EU Regulatory Affairs What would it mean to you to work for a regulatory authority or in the upper management of the crisis-proof pharmaceutical industry?
With this book, every newcomer can successfully enter the pharmaceutical regulatory business, because we have created a low-priced express solution for it. If you are searching for introductory literature on EU Regulatory Affairs and want to avoid expensive textbooks and courses, this book is your perfect starting point! Lean: You receive the exclusive tour around the fundamentals in only a few hours, which saves your valuable time. Superior Value: You buy the book for a moderate price and receive the know-how of a full university course in return. Navigation: Multi-year experts decrypt the most important key points and hand you the compass for a high-paying and fulfilling career. Competition-Boost: Secure the decisive advantage over competitors and establish yourself as the subject matter expert in your company.
No matter if you are a student or graduate, and you just feel lost coping with the job market after your academic career ends, or you’re preparing for an EU Regulatory Affairs class, certificate, or entry-level job interview, this book was designed to kickstart your success story in the field. Manager positions in Regulatory Affairs are well paid and have high job security, therefore they are in high demand and the competition is not sleeping.
However, with this book, we crafted a personal guide, fully at your disposal, just like a real-world colleague training you on the job, and that is simply invaluable. Not having this advantage due to indecision could cost you time and also job opportunities.
Enjoy the comfort of carefully compiled expert information, which only expensive professional or university education could give you. Skip through the noise and better invest your time and money in understanding the system from the ground up. The book covers topics like pharmaceutical development, European legal system fundamentals, pharmaceutical legislation, major players in the industry, marketing authorization applications, product lifecycle activities, the digital pharmaceutical dossier eCTD, quality, and much more.
EU Regulatory Affairs Made Easy offers you a clear introductory tour through the field, with expert insights, cross-references, weblinks, and a resources/glossary section. This book will save you hundreds of hours of research, on-the-job training, and traveling to expensive courses, since we are convinced that you shouldn’t spend between 10 to 20 thousand dollars or euros, just to fall asleep in a university master's program.
Steady job possibilities will wait for the ones gaining the positively “unfair” advantage over their competition, potentially making you the leading company expert in this field for your team or boss. Enjoy the exclusive insights our book will give you and develop an understanding that brings you results and income in practice.
Therefore, decide to boost your career NOW and secure your advantage in EU Regulatory Affairs. All it takes is one successful job interview. Make the decision now, because, in a year from now, where do you want to arrive?
Who knows, maybe you’ll become a regulator yourself in a couple of years?