Regulatory Medical Writing Training

Regulatory Medical Writing

Regulatory writing has become an integral part of the pharma landscape. Exponential growth in the sector has warranted tremendous increase in scientific and regulatory documents. These documents are a must for any pharmaceutical industry which they need to submit to regulatory authorities for a faster approval of their product (drug or device).
To fill this gap and provide high quality documents, a medical writing agency (with quality medical writers) could play a major role. These agencies help in quick regulatory submission and authorization and thus reduces the time lag which a product needs to reach the market. Professional and qualified regulatory medical writers with individual experiences of at least 2-3 years with different kind of documents (common technical document, case report forms, protocols, investigators brochure, informed consent forms etc.) form the pillars of such medical communication companies.
Turacoz Skill Development Program (TSDP), a wing of THS, provides basic and professional regulatory writing trainings. The entire 4-month course on 'Medical Writing and Pharmacovigilance' is set as per the current industry standards and encompasses recent guidelines, current trends and covers the fine technicalities of the regulatory medical writing. The main aim of TSDP is to bridge the prevailing gap in the pharma sector by providing quality regulatory medical writing training.