About the training Course
Aims and objectives
This training event will familiarize you with the regulatory affairs basic principles, regulations and standards. Participants will learn about the basic skills necessary to work with regulatory agencies (as: WHO, FDA, MOH). It addresses regulatory affairs specialist tasks’ and responsibilities’. You will know about bio therapeutic products.

Who may attend?
Do you need basic regulatory affairs expertise since you already work in the pharmaceutical industry or plan to start working in this field?
Then this training program is the fast track to becoming knowledgeable in this field.
No prior regulatory experience is required.

Training Topics

• Introduction to Regulatory Affairs.
• Regulatory Affairs Tasks & Responsibilities.
• Regulations, Regulatory Bodies and International references.
• Standards Applied to Regulatory Affairs.
• Types of Pharmaceutical Products.
• Biological Products.

Benefits

• Up-to-date expert knowledge
• Flexibility in attending and registration
• Post-evaluation and feedback
• Certificate of completion
• Training materials
• Top 3 attendees will be granted a free GCP training with certificates.
• Talented attendees will be invited for an interview at RAY-CRO.

Upon completion of the training
You will be conversant with the key principles of regulatory affairs and have a good starting basis to work in this field.
You will be granted a training certificate.