Regulatory Affairs plays a crucial role in the pharmaceutical industry, especially during drug development: a lengthy, complex, and extremely costly but necessary process.
Regulatory Affairs experts are involved in all phases of development, and even after drug approval and commercialization. They possess a unique combination of both scientific and management skills to achieve a commercially important goal within a drug development organization.
The Regulatory Affairs department provides strategic and technical advice at the highest level in such companies. In this way, they make a significant contribution, both commercially and scientifically, to the success of a development program and the company as a whole.
Many pharmaceutical companies are looking for external RA team members with specific expertise to ensure that products are developed, manufactured, and controlled at all levels of expected quality, safety, and efficacy. Experienced consultants to ensure all filing and submission goals are met, with high quality and within expected timelines.
Sounds familiar? This post will give you a better understanding of the role of Regulatory Affairs in the pharmaceutical industry at large and the functions that Regulatory Affairs teams can provide in the lifecycle management of your pharmaceutical product.
Be sure to read on!
