Clinical Research
 

Drug development is a complex activity that requires a broad array of medical and laboratory expertise, including toxicology, preclinical evaluation, clinical trial design and implementation. Today's drug development process has evolved through decades of scientific, technological and regulatory changes - all aimed at improving the safety and efficacy of new drugs before they come to market. As a consequence, it can take up to 12 years or more to bring a new therapy from discovery to market - a time consuming- capital - resource-intensive process. In face of this, many pharmaceutical, biotech and medical device companies look to outsourcing some or all of their drug development activities.

Through strategic outsourcing with Sristek, biopharmaceutical companies can access additional therapeutic and regulatory expertise, extensive clinical research experience, and state-of-the-art technology - without adding the associated fixed costs to clients R&D overhead.

Services
  • Phase I
  • Phase II-IV trials
  • Pharmacokinetic Studies
  • Feasibility Studies
  • Site/Investigator Identification and Selection
  • Project Planning and Setup
  • Study Design and Protocol Writing
  • Design & Development of CRF
  • Regulatory Affairs
  • Project Management
  • Clinical Monitoring
  • Clinical Study Site Management
  • Audit Services
  • Pharmacovigilance
  • Medical Writing
  • Clinical Data Management
  • Biostatistics & Clinical Programming
  • CRA/CTA/PM/Site Coordinator Outsourcing

Clinical Research

Clinical Data Management

Biostatistics and Clinical

Programming

Sristek Academy of Clinical

Research (SACR)

Staffing Solutions

 
 
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