Medical device registrar (RA) daily work is:
1, to complete the registration data preparation, collection, collation, reporting, follow-up work.
2, regular understanding of registration-related regulatory information.
3, to assist the company to complete the product type inspection , review, corporate standards modification work, and related departments to communicate with the relevant departments, to assist in completing the preparation of corporate standards, user manuals and other materials.
4, to complete the superior account of other related work.
The work is tired depends on your love for the work, if you love to do will not feel tired.
RA Regulatory Affairs (also known as medical registration in China), the work is centered around product registration. According to the company's business (product sales market) is different, divided into domestic registration and international registration, of course, there are also imported registration. Let's start with the daily work of an RA.
Medical device registration specialist prospects:
1, this should be the RA concerned about it. The important premise of wanting to develop in a company for a long time, so to speak, the bigger the pie, the bigger your share. The outlook is very good, as long as there are new medical device products are born, there is a need for registration specialist.
2, of course, not to say that every business is almost the same, just said just industry prospects. If it comes to personal prospects, then I will tell you that the prospects for personal development will not be too good, because the contact regulations and experience will be relatively little, no personal development and promotion space. This applies to any industry unless the company has unexpected circumstances and you are that good.