Our Values
We want to keep ‘medicines moving’ for everyone’s benefit, no matter who they are or where they are. In 2023, InViva has incorporated, to become a partnership, harnessing decades of shared professional industry experience. We love what we do and therefore recognise and care about the difference between high quality and average consultancy for our clients, minimising the risks that clients face, and undertake to offer you value for money, confidentiality and transparency at all times.
Our core regulatory services include
-
Pharmaceutical, medical device, combination product – regulatory affairs
-
GMP / Quality Management System – development, support, auditing
-
Project Management
-
New product development and technology transfer, including Intellectual Property strategy (using UK patent attorney partners)
-
UK Responsible Person assists with UKCA marking, and licence the use of our UK address
-
Clinical development advice
-
New product registrations across the world
-
Product licensing, ongoing licence maintenance
