Regulatory Science & Product Development Experts helping customers
Commercialise Products | Reduce Time to Market | Achieve Compliance | Grow Business
To Move your Program Forward….. Successfully !
The development of a new drug is a very complex, costly, and risky task. There are inherent difficulties in running a drug development programme successfully and the larger or the more innovative the project the more numerous potential problems can be. Applying function specific, modern project management principles to the development of products and product development activities is mandatory for successful, on-time and on-target delivery. Managing and Co-ordinating Product Development Programs and Projects can be an overwhelming and time-consuming task.
At Vyomus Consulting, our multidisciplinary team of expert drug developers and project managers facilitate a seamless transition between program planning, project management, implementation and execution to attain program goals within agreed upon service levels. Further, we have developed a flexible financial model that can facilitate your cash flows and significantly reduce your development budgets.
We start the engagement process by assigning a dedicated senior resource as a Program / Project Manager who would be the single point of contact throughout the process. The project manager controls and coordinates the complete process and approvals of all documentation which will ensure successful project delivery. Further, the project manager coordinates the decision-making process by identifying key issues and decisions that need to be made, and then ensures that you respond in a timely manner so as not to unnecessarily delay projects.
Our wealth of knowledge and experience will help ensure that your product is developed within an optimal timescale and budget since, at each stage of the project implementation lifecycle, Vyomus Consulting focuses on impacts and results for both business and functional stakeholders.
From discovery to commercialization, we design, implement and provide solutions specifically tailored to your business challenges which ensures significant return on investment and reduces total cost of ownership. Integrating Science, Regulations and Measurable Business outcomes, combining local knowledge with global standards, our team moves beyond providing expert advise to get your project off the ground and moving at a fast pace.
Our overall experience includes over six hundred preclinical, clinical trial approvals, product registrations, marketing authorizations, import and marketing authorizations, manufacturing and marketing authorization and transactions covering a large number of therapeutic and product categories.
We provide Project planning, Project execution, Project monitoring & control, Project closure services for Clinical development projects (Phase 1 to 4), Bioavailability & Bioequivalence projects, Clinical Data Management Projects, Pharmacovigilance projects, Validation projects, Outsourcing initiatives etc.,