Guru Murthy Email & Phone Number

Planning, coordinating and review regulatory submissions to support Global Regulatory by providing appropriate components for Regulatory dossiers.• Understanding of regulations, guidelines and developing procedures and policies relating to registration and manufacturing of pharmaceutical products, to expedite submission, review and approval of global regulatory applications.• Works across the functions and can work with Stakeholders in development functions in provision of advice interpretation of relevant guidance’s, researching topics and resolving issues.• Dossier review responsibilities for the peer and identify improvement opportunities for Regulatory processes to ensure dossier is fit for purpose.• Drive the submission and delivery process with the Global Publishing team to ensure timely dispatch and archival of submissions as per the agreed timelines.• Manages multiple project assignments (e.g., Variations

Listed skills include Powerpoint, Windows, Gmp, Clinical Research, and 15 others.