Is pharmaceutical regulatory affairs a good career?
Along with the promise of job security, pursuing a career in regulatory affairs affords you a great deal of flexibility in where you choose to work. As of 2018, 73 percent of regulatory professionals work directly in a regulated industry, such as pharmaceuticals, medical devices, biotechnology, or food science.
What does regulatory affairs do in pharma?
Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. They are often employed by pharmaceutical, biotechnology, and medical device companies.
What do Regulatory Affairs earn?
How much does a Regulatory Affairs Specialist I make in California? The average Regulatory Affairs Specialist I salary in California is $69,625 as of July 28, 2021, but the range typically falls between $60,735 and $78,368.
What is Regulatory Affairs certification?
The Regulatory Affairs Certification (RAC) is the only credential for regulatory professionals in the healthcare product sector. The certification demonstrates to employers, clients and colleagues essential knowledge, critical thinking abilities and a commitment to continuing professional development.
What is a pharmaceutical certification?
Certificate of pharmaceutical product. Jump to navigation Jump to search. The certificate of pharmaceutical product (abbreviated: CPP) is a certificate issued in the format recommended by the World Health Organization (WHO), which establishes the status of the pharmaceutical product and of the applicant for this certificate in the exporting country.
What is a regulatory specialist?
Job Description for Regulatory Specialist. Regulatory specialists work with regulatory procedures and bodies, with day-to-day functions including writing and auditing reports and applications, as well as verifying and recording the company’s progress. In addition to producing reports, the regulatory specialist must contribute to analyzing company…
