Our services.

 

NEW SITE/INVESTIGATOR DEVELOPMENT

Establishing a research department in your practice can be daunting, time consuming, and costly. All that and no guaranteed return on your investment. With Titan Medical Research as your partner, we will remove all of those burdens. Over time we will grow your research portfolio into a consistent revenue generator that provides your patients access to safe, cutting edge medicines and procedures, at no cost to you. We handle every step from start to finish. Here is a brief list of some of the services that entails:

  1. Study acquisition (study identification, CDA execution, protocol feasibility, site selection and initiation, contract negotiation, regulatory and startup process, source document generation).

  2. Study execution (subject identification and recruitment, study visits, monitoring visits and correspondence, drug/device accountability, data entry, query resolution, quality assurance, marketing and advertising).

  3. Study close-out (record archiving, correspondence, monitor visits).

 

EXISTING SITE/INVESTIGATOR

For a practice that has an established research portfolio but is looking to optimize revenue generation while simultaneously minimizing burden, Titan offers a scalable solution. From consulting services to help boost your efficiency in key areas, to a complete migration to Titan Medical Research, we will find the solution for you and at no cost. The areas that we can assist you in include (but are not limited to):

  1. SOP development. Drug companies are looking for sites with established processes and protocols that assure research can be conducted safely and effectively. We will ensure your SOP is optimized to attract the studies you want, and to allow your team to operate to its fullest potential.

  2. Study identification and selection. Titan has the necessary industry contacts and processes in place to find studies that fit your patient population, and accelerate through the process of adding them to your research portfolio.

  3. Administrative and regulatory management. We can track patient visits, invoice study payments, and leveraging our experience with a variety of sponsors, CROs, and IRBs, we will ensure your studies are running as efficiently as possible.