Shrutika Chillal joins DRA as a Senior Regulatory Publisher with experience in managing regulatory submissions ensuring compliance with global regulations and optimizing submission process. Ms. Chillal is proficient in compiling and formatting regulatory dossiers, including clinical trial data, safety reports, and labelling information, in accordance with regulatory requirements.
Prior to joining DRA, she was a Senior Regulatory Operations Associate and was involved in planning, publishing and submission of INDs, NDAs, BLA and MAA. Ms. Chillal also has experience in protocol registration and disclosure of results on clinical trials.gov and EudraCT, as well as in developing SOPs and work instructions, and providing training to team members.