Comprehensive Regulatory Affairs Database of Pharmaceutical Regulatory Oceania

This database includes a complete profile of the various pharmaceutical regulatory systems in sovereign countries located across the Oceania region; specifically from the point of view of a regulatory affairs professional. The database contains a total of 89 standardized regulatory parameters which include items such as authority to regulate, frame of proposed regulation, marketing authorization options, clinical trials, post-market surveillance, GMP compliance, and many more. The database is designed so that the regulatory frameworks of each country can be compared on a systematic basis and helps provide information to develop regulatory strategies; plans to commence doing business in an Oceania country; develop regulatory documents to submit to a regulatory authority; compliance assessments; and conduct academic research. The database can also be used as a point of reference for pharmaceutical companies; regulatory professionals; researchers; and students who are looking for country specific regulatory intelligence for each country in the greater Oceania region.