About Us
Intouch Clinical Research Center is well-known to the Pharmaceutical Industry as an SMO [Site Management Organization] and having a singular focus on conducting Ophthalmic clinical trials at the highest level of quality and ethics.
Vision of Intouch Clinical Research Center:
• Work closely with you to establish a partnership and develop the clinical research capacity of your practice
• Be on the cutting edge of developing new/better Ophthalmic products and treatments
• Bring about opportunities to author prestigious journals based upon the clinical research studies conducted at your clinic
• Help bring new patients to your practice through their participation in research studies
Areas of research interest include:
• Dry Eye Syndrome
• Refractive Surgery
• Cataract Extraction with lntraocular Lens Implantation
• Ocular Consumer Products and Contact Lenses
• Anti-lnfectives
• Retinal disorders
• Uveitis
• Meibomian Gland Disease/ Blepharitis
• Anti-Inflammatory products
• Glaucoma/Ocular Hypertension
Intouch Clinical Research Center- What do we provide?
A Site Management Organization (SMO) is an organization that provides clinical trial related services to a contract research organization (CRO), a pharmaceutical company, a biotechnology company, a medical device company or a clinical site. The site is usually a hospital or a similar health care institution that has adequate infrastructure and staff to meet the requirements of the clinical trial protocol. The scope of an SMO's responsibility is limited to the 'site' and hence the eponymous title. Some (but not all) of the responsibilities include:
· Contract
· Submission for Institutional Review Board or Independent Ethics Committee (IRB/IEC) approval.
· Patient Counseling
· Patient Recruitment
· Patient Follow-up
· Informed consent form (ICF)
· Site initiation and trial close-out operations
· Trial-related documents archival and maintenance
· Reporting serious adverse events to the Sponsor or CRO and the IRB/IEC
· Ensuring protocol compliance
· Advising & alerting investigators of potential protocol violations
· Advising & alerting investigators of potential ICH-GCP violations
· Provide trained and highly-qualified Clinical Research Coordinators
Vision of Intouch Clinical Research Center:
• Work closely with you to establish a partnership and develop the clinical research capacity of your practice
• Be on the cutting edge of developing new/better Ophthalmic products and treatments
• Bring about opportunities to author prestigious journals based upon the clinical research studies conducted at your clinic
• Help bring new patients to your practice through their participation in research studies
Areas of research interest include:
• Dry Eye Syndrome
• Refractive Surgery
• Cataract Extraction with lntraocular Lens Implantation
• Ocular Consumer Products and Contact Lenses
• Anti-lnfectives
• Retinal disorders
• Uveitis
• Meibomian Gland Disease/ Blepharitis
• Anti-Inflammatory products
• Glaucoma/Ocular Hypertension
Intouch Clinical Research Center- What do we provide?
A Site Management Organization (SMO) is an organization that provides clinical trial related services to a contract research organization (CRO), a pharmaceutical company, a biotechnology company, a medical device company or a clinical site. The site is usually a hospital or a similar health care institution that has adequate infrastructure and staff to meet the requirements of the clinical trial protocol. The scope of an SMO's responsibility is limited to the 'site' and hence the eponymous title. Some (but not all) of the responsibilities include:
· Contract
· Submission for Institutional Review Board or Independent Ethics Committee (IRB/IEC) approval.
· Patient Counseling
· Patient Recruitment
· Patient Follow-up
· Informed consent form (ICF)
· Site initiation and trial close-out operations
· Trial-related documents archival and maintenance
· Reporting serious adverse events to the Sponsor or CRO and the IRB/IEC
· Ensuring protocol compliance
· Advising & alerting investigators of potential protocol violations
· Advising & alerting investigators of potential ICH-GCP violations
· Provide trained and highly-qualified Clinical Research Coordinators
Clients• Alcon
• Shire • Eleven Pharmaceutical • Allergan • Sarcode • Bausch & Lomb • Ocular Therapeutics • Kala Pharmaceutical • Senju Pharmaceutical • Santen Inc. • Lexitas Pharma (CRO) • ProTrials (CRO) • Trial Runners (CRO) • Auven (CRO) • Inc Research (CRO) • Syneos Health (CRO) • Quintiles (CRO) • IQVIA Health (CRO) |
Interviews |