At Ixia Clinical we are highly experienced at dealing with regulatory boards and ethics committees, having forged strong and lasting relationships with several institutional bodies. We are experts in skilfully navigating the requirements for the preparation and submission of trials for ethical and regulatory consideration in the shortest possible timeframes.

Our team can either provide support to your regulatory operations or take charge and manage the entire approvals process. This can be done at all phases of the product life-cycle. We are flexible to meet the needs of your project and can advise on the most effective solutions and strategies to achieve your project objectives.