Agati listens to each client’s specific needs for clinical talent, whether it is for one individual or for a functional team, we can assemble the right solution for each situation.  We specialize in global placement of CRAs, CTMs, Project Managers, Study Start up Specialists, SWAT CRA teams, Safety Associates, Site contracts/payments administrators, auditors and other critical roles that support your highest priority clinical programs.  We can place staff part-time, full-time, temp-to-perm meeting your requirements.

Agati’s medical writers have a strong academic, pharmaceutical and biotechnology industry background and can help clients’ prepare clear, concise and high quality

The FSP model allows separation of core/non-core capabilities within your company allowing you to choose providers specializing in a discipline e.g. Statistical Programming, Biostatistics, Data Management, Regulatory and Pharmacovigilance.

Our experienced Statisticians and Statistical Programmers help our customers in analysis of clinical trials of all types including parallel, crossover, multi-phase and PK/PD studies. Our statisticians programmers are committed to follow SOPs and ICH guidelines. We are flexible in producing reports in sponsor-defined templates or usingour standard templates

In a highly regulated and ever changing regulatory environment our eCTD submissions publishing experts make sure pharmaceutical companies’ submissions publishing requirements are fulfilled comprehensively. We help our clients navigate through FDA’s eDRL SPL process with guaranteed 100% accuracy. 

Our highly skilled developers bring to the fore in-depth IT expertise that extends across various platforms and domains, providing you with turnkey assistance to execute your end-to-end application design needs at lesser costs and with shortened development cycles.

Agati Clinical provides the experienced Data Management team which has the capability to work on any EDC platform and on bespoke customer platform as well. Due to the complete understanding of end to end processes, our team can suggest the right solutions to the problems with an eye for detail, resulting in total customer satisfaction. 

We have an extensive experience delivering end-to-end services in the area of Pharmacovigilance KPO.  Our PV KPO practice has rich experience of handling annual volumes of more than 100,000 cases. We ensure metrics-driven delivery of business processes from strategic global delivery locations across the U.S & India.