• Study design consultation
• Submission of application for EC approval
• Protocol development
• Assistance with site and investigator documentation

• Support with identification and set-up of viable study sites
• Staff training on procedures, devices, and documentation
• Management of all on site study activities
• Customer helpline 24*7 and 365 days

• Study drug administration (IM, IV infusion or Subcutaneous)
• Biological sample collections (e.g. nasopharyngeal, nasal or oral swab collection, urine collection)
• Blood sample collection
• Transporting the specimen from patient home to site
• Maintaining cold chain for transportation
• Clinical assessment and support by qualified professionals
• Source documentation and questionnaire development and utilization
• Patient training and education

• Strong internal quality assurance [QA] review
• Standardized clinical and operational practices
• GCP training and adherence to all local and national compliance standards

• Licensed to import of special equipment needed for trials
• Storage in temperature-controlled facilities of test kits
• Cold chain logistics for shipment of samples
• Assistance for ensuring availability of commercial products and devices and ancillary supplies

• Registered nurses available for clinical support at home (drug administration, medical tests, reminders)
• Patient education, support and counseling
• 24*7 call center for customer support
• Patient assistance for PSP required hospital and doctor’s visits
• Patient assessment at home or remotely
• Consistent, compassionate, one on one engagement with patients, which increases the retention of patients
• Chaperone services for patient

With on-the-ground experience in undertaking clinical trials for both local and international pharmaceutical companies, we work in partnership with investigators undertaking IIS, offering seamless clinical and operational support that enables the investigator to run clinical trials in their areas of interest and to generate results and collate relevant patient and drug data both efficiently and effectively.

Avatar provides structured, experienced support for investigators. For single or multi-site trials, our highly qualified clinical team are equipped with the experience, training, diligence, and compassion required to offer both the investigator and study participants confidence in the services provided. Avatar’s professional support allows investigators to confidently lead their study by relieving them of concerns around the care and management of study participants, thereby giving investigators more time to process, manage, and analyze the critical information collected during the study and make it a success.

We Offer…

• Relevant and diverse clinical and operational on-the-ground experience.
• Consistent and transparent communication throughout the entire course of the IIS trial, on your terms.
• 24*7 Support with the patient recruitment process, if required.
• The ability to support multi-site study coordination, across India.
• The ability to work with investigators to identify international opportunities for IIS project submission.
• HIPPA/GDPR compliance.