Get comprehensive phase 1 to phase 4 clinical trial services (planning to reporting). Trust in a proven track record of successful partnering on the design of quality research and delivery of data.
Leading the way to timely clinical trial approvals.
Our international team of regulatory professionals help transition multi-national clinical trials from concept to implementation by navigating complex regulatory environments and ensuring quality and timely submissions.
Working cross-functionally with other operational departments, the RA group provides important regulatory intelligence to the build out of the ideal start-up strategy for global clinical trials. Complex regulatory environments in North America, Europe and Asia-Pacific are well-understood and effectively navigated to ensure optimal regulatory and ethics approval timelines.
With regulatory intelligence built on insight and experience in over 30 countries in Europe, North America and Asia-Pacific, Regulatory Affairs at Alimentiv will provide regionally and therapeutically-based considerations to support effective regulatory start-up strategies.
Alimentiv has secured a network of established partnerships across the world to allow for seamless regulatory support and services in a growing number of regions.
Alimentiv Regulatory Affairs leverages a depth of internal therapeutic knowledge to connect drug development with clinical trial submission strategies.
Putting a strategy into motion through effective planning, preparation and execution of multinational clinical trial submissions.
All projects are supported by Alimentiv’s large repository of country submission specifications and requirements.
The principles described above are applied to all clinical trial regulatory activities, including:
Regulatory Affairs at Alimentiv will manage and oversee the submission process from protocol completion through end of study reporting. This is accomplished through adequate planning and prioritizing sponsor engagement by utilizing tools to ensure transparent and frequent communication and reporting of all regulatory activities throughout the lifecycle of the project. Information flow from the sponsor and other vendors through to the local teams is closely managed to ensure timely and quality submissions.