Free training and meeting

Training remote or on-site (in-house)

We believe face to face training either in a webinar or on-site (in-house) training to get Chinese regulation familiar in your regulatory group.

How many take away messages are left after reading a monthly newsletter or group webinar in group? It is matter of fact without a prove of this “passive” learning it is just an "experience".

In our free webinar you are sitting alone or with your colleague on the side, either as Junior or Senior regulatory affairs manager. You get firstly briefly what is basic Chinese regulation of medical device or IVD. Afterwards it is your element; we discuss the trouble in your established company-process and try to provide scenarios of paths to solve the trouble. 

It is not always smooth in Chinese and international project. Join our training "how to deal with chinese and international partners". Our raising popular training is "Regulatory Affairs Lean" with many intelligent insights how to make daily work efficiently and agile.

You will learn how to leverage and control Chinese project with KPI. Mastering communication with international stakeholders is cost-saving. Negotiating with authority can accelerate the market entrance of your product.

Q&A session with second premium voice

You might work constantly with one registration service partner or hear different opinions of regulatory hurdles from familiar stakeholders. We bring neutral expertise of your trouble transparently.

It is always better to adjust problem in a professional ways in a meeting than writing only emails. It is wise to have a kind of project controlling whether your solution is the best choice and more important how to set this solution in your procedure to reproduce the success.

We have elite records to write "expert opinion" (2-3 h efforts within one week) after an effective meeting.

The costs start only if you agree with our analysis of solutions.