What is the meaning of RAC?

RAC stands for "Regulatory Affairs Certification".

This certification program is especially for the candidates who are willing to get admitted in the healthcare sector. They are then allotted in the different departments such as consultancies, regulatory agencies, and other various departments related to such fields.

But to notice, there are actually two tests, that is RAC drugs and RAC devices. This test falls under the regulatory agency of Regulatory Affairs which promotes expertise in the two sectors, pharmaceuticals as well as medical devices. An individual can choose between the two tests since both the tests have the same value and the qualifying candidate will have the opportunity to add ‘RAC’ after their name as a tribute.

The course is of three years of period. Each selected candidate is given certain responsibility that would allow them to have experience in the respective field. Each year, the format is revised, and new strategies are implemented.

This test is holding value in the medical world. It promotes a candidate’s ability and adds high value to the portfolio, and also unravels better career opportunities.

Background:

The Regulatory Affairs Certification Board (RACB) oversees the development of the RAC examinations. Each examination is developed by an examination committee comprised of practicing regulatory experts knowledgeable about the relevant regulations for the region.

The RAC examinations are based on job analysis studies undertaken by the RAC program. These studies are guided by experts in testing and measurement. The job analysis studies are completed before an examination is created and repeated as needed to determine whether there are changes in the role and scope of practice of regulatory professionals that would require adjustment of the examination content. The job analysis study is used to develop the content outline for each examination and determine the number and type of questions to be included in each content area.