Kinapse is organised into three service lines; Post-approval Regulatory, Post-approval Pharmacovigilance and Development Operations (Clinical Trial Disclosure and Medical Writing)
Our Regulatory team deliver full strategic and operational Regulatory services on a global scale.
We provide full service support in Safety & Pharmacovigilance covering all pre and post approvals.
Our strength and depth in Clinical Operations ensures the successful delivery of all projects.
Get in touch with our expert team