Hello,
I have been in Regulatory Affairs for a medical device for last 3 years and know reasonably well about the regualtory affairs for US markets. Now my company wants me to lead the regualtory Affairs of US aqnd Europe activities and want me to be a champion and to lead in our company.
In this regards, would some one help me to define the relevant training and certification required to be "competent" in this field ?
Thank you in advance
I have been in Regulatory Affairs for a medical device for last 3 years and know reasonably well about the regualtory affairs for US markets. Now my company wants me to lead the regualtory Affairs of US aqnd Europe activities and want me to be a champion and to lead in our company.
In this regards, would some one help me to define the relevant training and certification required to be "competent" in this field ?
Thank you in advance