Phase I:

Safety assessment after evaluating the following parameters on normal, healthy volunteers.

Primary outcome measures: AEs, Ocular Comfort Index

Secondary outcome measures: Visual acuity, Epithelial defects – Fluorescein stain, green lissamine, conjunctival hyperemia, chemosis.

Phase II:

Safety and efficacy on a small population to evaluate and investigate the treatment effect on subjects with defined conditions.

Phase III:

Benchmark controlled safety and efficacy study on subjects with defined conditions.Large sample sizes.

These studies are designed in a scientific and robust manner and include ophthalmological examinations with a standard/ published scale along with instrumental imaging and high quality imaging to record visible differences. The study may also be combined with biological sample collection and analysis as required.

Subjects with the following ophthalmological conditions can be recruited

Age-related macular degeneration

Geographic atrophy

Blepharitis-15-20 per month

Cataract lenses- 20-25 per month,

Conjunctivitis[ viral/ bacterial/ non specific/infective/ allergic/ non-infective] Such as Ocular adenovirus infection

Contact lens solutions: Quality, tolerance and comfort

Diabetic macular oedema

Dry eye- clinical examination, quality and quantity of tear/ Intraocular lenses

Post-cataract surgery maintenance

Sjorgen’s syndrome


Ocular burns- chemical injury

Corneal foreign body

Retinitis pigmentosa


Vitreous implants-costly implants [ A corrective treatment for diabetic macular edema]

Diabetic retinopathy

Acanthamoeba keratitis- Mostly seen in, contact lens users

Ethics Committee

Independent Ethics Committee
Registered with CDSCO
Strictly follows Clinical trial guidelines and quality policies
Weekly review meetings

Study Management Services

Our team of 50+ trained professionals has extensive experience in managing clinical studies for sponsors across the world.
Our services include but are not limited to:

  • Scientific Consultation
  • Protocol Development
  • Medical Writing
  • Comprehensive Project Management
  • Multicentric Study Coordination and Management
  • Clinical Monitoring
  • Medical Monitoring
  • Data Management
  • Biostatistics
  • Reporting