At Lotus Labs, we understand the imperative for expediting drug development programmers so as to adhere to established milestones and budgetary parameters. The Regulatory Submission Teams at Lotus Labs are committed to ensuring best-in-class regulatory services that draw deeply from our wide experience in regulatory affairs. Sound knowledge of regulatory requirements, international norms and vast experience of interacting with renowned global regulatory bodies enable us to ensure quality and reliable compliance with regards to study submissions. The regulatory submission activities include Formulation of regulatory strategies, Compilation of the clinical trial application, Submission and follow-up of the application, Response to regulatory agency queries, Procurement of drug import licenses, Procurement of NOC for export of biological samples and many more as required by the sponsor.