ARPA offers different RA certificate courses in more than 10 universities in Asia.
We also provide trainings to regulators in more than 5 countries
ARPA has 2 major publications for our trainings and good practice sharing
Contact us if you are interested to contribute articles
Handbook of Medical Device Regulatory Affairs in Asia. (2nd Edition now)
This is the textbook that includes contributions from many experts in government, standard organisations and industries
It is available in many online bookshops
Asia Health Care Journal
You can download from the following Healthcare Federation link
(Contact us if you are interested to contribute articles)
ARPA presents awards to students in our teaching universities for good regulatory performance
Contact us if you are interested to sponsor our award
ARPA creates standard to enhance our professionalism
We have drafted a procedure on how to audit RA department. Contact us if you want a copy (free of charge)
Good Regulatory Practice Research Centre
With support of China Food and Drug College, a GRP Research Centre was established
to support research on good regulatory practice
In Hong Kong, the LRP Panel meeting and regulatory forum is open for public to share the latest Hong Kong and regional regulatory updates. We also use the forum to share updates from Asian Harmonization Working Party (AHWP) by industry (non-governmental organization) and government representatives.
Prof Raymond Tong is our Forum Chair.
Please find below the link of our forum meeting minutes and presentation slides
ARPA is working with an expert panel from government, industry and academia to develop a summary of Medical Device Registration requirement, approval time, fee required
Please complete the database request page below to get the information
If you find that our Medical Device Registration Requirement summary needs correction, please contact Jack Wong (firstname.lastname@example.org)