Devara Srikanth Email & Phone Number

• Preparing the regulatory dossiers for health authorities of the EU. performing documents, bookmarking, hyperlinking, submission and Publishing level activities.• Good knowledge in regional eCTD guidelines.• Good knowledge on Europe procedures response timelines i.e. DCP, MRP and National.• Performing publishing level activities like complation of dossier, submission through eCTD to various health authorities.• Full hands publishing tools like eCTD, Global eCTD, Lorenz eValidator and CESP.• Preparation of responses to agency and customer queries, responding with the given timelines. • Responsible for maintaining the product quality trackers and monthly status updates.I am sarching out to you all to let me know if you have any suitable job openings for me in your company or have any references.The preferred Regulatory affairs where I can contribute to the organization to expand my knowledge and utilize my learning skills.