A clinical research consultancy that builds and operates.
Tamam Solutions exists for organizations that need to do clinical research and do not have the research function to do it, or do not have enough of one. For hospitals and clinics, we build that function. For sponsors, we are that function, or an extension of the one they have.
What we believe
Good research is mostly good infrastructure.
The science gets the attention, but studies succeed or fail on procedure. Was consent documented properly? Did the IRB have what it needed? Does the data that was captured match the analysis that was planned? Could the site actually deliver what the protocol asked for? We treat that infrastructure as the product.
We hold ourselves to the same standard a regulator or an IRB would. That means careful wording, no claims we cannot support, and documentation that says what was done.
Why both sides
Most firms in this space serve one side of the study. Consultancies help institutions build compliance programs, and CROs run studies for sponsors. We do both deliberately, because the two problems are really the same problem seen from different chairs.
A site is only research-active if sponsors will place studies there, so the procedures we write for a hospital are built to pass a sponsor's qualification visit. A sponsor's study only succeeds if sites can execute it, so the protocols we write are built around what a coordinator can actually do. Working on both sides keeps us honest about each.
We are currently supporting active trials with early-stage sponsors alongside our site-infrastructure work.
How we work
- The deliverable is the infrastructure.SOPs, policies, protocols, forms, and submissions that someone can pick up and use, rather than a deck of recommendations.
- Continuity from start to close.The people you meet in the first conversation are the people who do the work, all the way through activation or closeout.
- Built to be run without us.Everything we build for a site is designed for your staff to operate. Everything we build for a sponsor is delivered in a form you can take anywhere.
- Written to the standard reviewers apply.45 CFR 46, 21 CFR Parts 50, 56, 312 and 812, ICH E6(R3), and the AAHRPP standards are where we start, not where we hope to end up.
- Only work we can do well.If we are not the right team, we say so in the first conversation.
Our team
Our team covers what an engagement needs: regulatory affairs and human research protections, protocol and instrument design, clinical operations and site management, and data capture and management. We size the team to the work rather than the other way around, and a senior lead owns every engagement.
Work with us.
Whether you are a site or a sponsor, the first step is the same. Tell us what you are trying to do.