Our mission is to provide the highest quality consulting services to all our clients in the Pharmaceutical medicines and devices sector. We emphasise a commitment to client satisfaction via appointment of our accomplished consultants to all projects.
– Required if clinical trial sites in the EU and no legal EU presence
– Useful if no legal entity within the EU
– To hold product designations, e.g. orphan drug, and marketing authorisations
– Advice on compliance with EU General Data Protection Regulation
– Prepare templates for obligatory documents e.g. Data Protection Policy, 3rd party Data Protection Agreement, Investigator Site Agreement
– Data Protection Officer services including point of contact in EU, Data Protection Impact Assessment, audit and compliance
We support our clients throughout world, including the EU and UK, North and South America.
We use innovative IT to support our communications and our team:
For a brief, free-of-charge discussion about specific project-related problems or issues, feel free to email us at:
Associates: Pharma Data Protection