Pharmacovigilance is a sub field of Pharmacy which includes research, detection, assessment and analysing the drug’s safety or safety of medicinal products. It is a very popular course in Medical Science. This course is suitable for the candidates who wish to join any pharmaceutical industry or pursue research in the future.
Live sessions with
Practical Exposure with a CRO
Soft Skills Training
This Program would help you to gain in-depth knowledge on the best way to collect and report adverse events and safety data and manage the risk associated with and risk to pharmaceutical products. Its unique format will provide you with the key skills and knowledge needed to operate a fast, effective drug safety or pharmacovigilance program.
I was looking for an opportunity to learn more about medical writing before starting my career in clinical research. The training helped me to understand medical writing from the grass-root level leading me to perform various activities efficiently within a short time span. The training starts with basic learning and gradually shifted to advance learning as per my comfort and capability.
It was a great experience for me and yes I have gained a lot of knowledge like protocol writing, safety narrative writing, CSR & interview skills and how this course and training plays a vital role in career growth. So the aggregate is that it really matters what I gained from this training program.
This training has helped me to build up my skills which I was not even aware off. I am really grateful that I enrolled for this training. I am thankful to you for being our mentor and guiding us at every step in this training.
I am Mahaprasad from Xavier University want to state that, it was a wonderful experience for me to get training, it was a privilege for me that you were my mentor, throughout the session who guided and supported me a lot. And once again thank you so much.
Thank you, you are inspiration for us, your knowledge, experience and behaviour are amazing, we learnt a lot from this training.
The evolution of clinical research is a long and fascinating journey. The history of clinical research accounts for the high ethical, scientific, and regulatory standards represented in current practice. In this module students will understand how it all began and evolve.
Regulatory medical writing is for clinical research document preparation. It is important for students to have the in-depth understanding of the various aspects of clinical research.
Good clinical practice (GCP) is an international ethical and scientific quality standard for designing, recording and reporting clinical trials that involve the participation of human subjects. It is important for students to understand the principals of GCP and its implementations. This module will help students to understand the various aspects of GCP in clinical research.