Regulatory affairs courses

...An Overview of Pharmaceutical Regulatory Affairs for Support Staff. Key Topics to be be covered:- Understand the Background of EU Law – Regulations, Directives and Guidelines Discover where you can find Information on Regulatory Affairs, Approvals, Withdrawals etc Assess the Impact of the... Learn about: Directives etc, EU Law, IT Law...

... by the latest legislation. This interactive course will guide you through national procedures as well as exploring the implications of and updates on the Eurasian Union regulation. The focus of the programme is to offer practical advice in developing your regulatory strategy for product approval in these... Learn about: Pharmaceutical Management, Regulatory Affairs, Russian regulatory affairs...

... of appropriate examples as well as an understanding of how the regulatory framework is intertwined with practical and scientific considerations. Thus the programme emphasises the acquisition of practical scientific skills as well as up-to-date theoretical knowledge in the area of pharmaceutical science... Learn about: Pharmaceutical Science, Molecular Sciences, Experimental Techniques...

...This 2 day course provides a detailed description of how analytical methods are validated, enabling a full understanding of method performance characteristics and associated statistics and how they are applied. This knowledge will enable informed interpretation of the regulatory guidance... Learn about: Either to design and carry out the investigation, Quality assurance managers, Quality control analysts/managers...

... of the regulatory aspects of site inspections •Requirements for the marketing of NCE, Biologic and biotechnology products, generic drugs and OTC medicines... Learn about: Life Science, Medical training, Pharmaceutical Marketing...

... Regulatory Affairs and Current issues, this will give you a broad introduction to the subjects related to it. Furthermore, you will learn about the Food Regulatory Affairs in India (FSSAI, Approvals etc.), a more specific approach to these regulations. And last but not least, you will learn about the... Learn about: Risk Analysis, International Food Regulatory Affairs, IT risk...

... and up-to-date knowledge and skills. This Advanced Clinical Research and Regulatory Affairs training program is practically driven and centered on the tasks expected of a regulatory affairs professional in the clinical research industry. In this Regulatory Affairs training you are provided with the understanding... Learn about: Clinical Research, Therapeutic AREAS, Medical training...

...The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs... Learn about: Patent Law, Industrial IPR Design &Trademark, IT industry...

... you with an understanding of the key areas of regulatory affairs in the region, a focus on the practical aspects to assist with regulatory activities. Also the opportunity for you to participate in interactive discussions and exchange experiences with other delegates... Learn about: French Speaking, Medical Science, Pharmaceutical Regulations...

... countries and you will enhance your knowledge and skills in the field of Regulatory affairs. The objectives of this course are to create experts in the field of RA documentation and research, to encourage continuous learning and development in RA field and to update knowledge of existing RA professionals... Learn about: Regulatory Affairs, Pharmacy Technician, Pharmaceutical Marketing...

...This recorded webcast series focuses on the main legal challenges in regulatory affairs. Participants will get a thorough understanding of the legal impact of processes in the marketing authorisation phase as well as throughout the life cycle... Learn about: Operational Risk, Operations Management, Change Management...

... treatments to the marketplace. Pharmaceutical physicians need excellent inter-personal skills to coordinate their research and development efforts with other industry experts, organisations and regulatory agencies worldwide. The goal of the online Pharmaceutical Medicine program conducted by James... Learn about: Drug Discovery, Medical training, Regulatory Affairs...

...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Drug Interaction, Regulatory safety, Drug Metabolism...

...Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in regulatory affairs is required... Learn about: Pharmaceutical manufacturing, Regulatory Compliance, Pharmacy Assistant...

... requirements for Russia, Kazakhstan, Belarus and Ukraine, particularly with regard to CMC. You will also be able to prepare the CTD dossier, especially Module 3 and the normative document for Russia. Moreover, you will be familiar with the change management requirements to achieve regulatory and GMP compliance... Learn about: Operational Risk, Operations Management, Change Management...

...Import Brokers Prior Notice Information CBP and FDA computer programs Import Codes Bonds and Bonded Warehouses FDA "Notice of Action" Lecture... Learn about: Regulatory Compliance, Regulatory affairs managers, Domestic cleaning...

...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Drug Development, Clinical management, Clinical Trial...

... will acquire skills in Regulatory Affairs, Regulatory Compliance, Regulation Law and more! This is your opportunity to enrol in such an amazing programme! Learn more about this course now! Just contact Indian Biological-science and Research Institute through Emagsiter.co... Learn about: Health Visitor, Regulatory Compliance, Regulatory Affairs...

... scientific practice. You’ll begin by focusing on advanced pharmaceutical skills; including dosage, approaches and techniques, before moving on to the pathway of a drug from its initial discovery to extensive clinical trials and regulatory approval. Let our SuperLabs and nanotechnology research lab become... Learn about: Problem Solving, Pharmaceutical Marketing, Pharmaceutical manufacturing...

...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Fundamentals of Clinical Trials, Drug Designing, Drug Interaction...