Let us manage your contracting, so that you can focus on the other critical study conduct aspects
Site contracting can be quite a challenge, especially when multiple countries are involved. Find out how our international team of experienced and dedicated lawyers can contribute to a smooth study start-up process.
Start a timely conversation on what contracts are required for your clinical study, and how to incorporate contracting in your budget and planning.
Contact us in case you need support with resolving a dispute with your contract counterpart. We might be able to assist when a solution seems far away.
The success of a clinical trial very much depends on the performance of critical study aspects by the different parties involved. Proper vendor contracting can make all the difference.
Find out how GDPR and other data privacy requirements apply to your organization and clinical study, and what solutions can be offered to ensure compliance.
Specific contract types, such as licensing agreements or consortium agreements, require legal review by a party with industry knowledge.
The same applies to study documents such as Patient Informed Consent Forms (PICF) or Letters of Delegation (LoD).
Biotech / Small Pharma
Karpervijver 143703 CJ ZeistThe Netherlands+31 (0)30 303 firstname.lastname@example.org
Salvius Legal BVKVK 51665174
© 2023 Salvius. Salvius Legal BV - KVK 51665174
Your global partner for clinical contract solutions