Clinical Trial Services

Sainalytics provides expert clinical trial services to the pharmaceutical and biotechnology industry. Our staffs are skilled in clinical trial management, clinical monitoring, expedited study start-up, patient recruitment, and the execution of study feasibility assessments. Sainalytics prides itself in being able to skillfully execute the vital operational best practices needed to ensure that your trial is conducted according to your time, quality, and cost objectives.

Clinical operations are a critical component in all studies. From start-up to close-out, our highly skilled clinical operations teams ensure proper planning, conduct, patient safety, and data quality, while fostering good communication between study sites and sponsors.

Whether helping with an overload of work or designing a full-service clinical program, our experienced, knowledgeable team is ready to partner with you to develop a program customized to your needs.

Sainalytics clinical trial services include:

  • Strategic Development Plans
  • Phase I, II, III & IV Protocol Development
  • Study Document Preparation
  • Investigator Brochure Preparation
  • Source Document and CRF Design
  • Third-party vendor management

Sainalytics clinical development programs meet the highest standards of the pharmaceutical, biotech and device industries, and comply with all industry requirements, and applicable local and national laws, rules, guidelines and regulations. At Sainalytics, we maintain the highest standards in working for clients, resulting in higher client retention rates. We strive to move our clients towards their goals efficiently and with greater success.

We’re your best partner. Our goal is to provide you with the services that best meet your needs, and responsible trial monitoring handled by experts. Tell us your challenges - we’ll help you determine your best course of action.