How Can PharmOcu help you?

Pharmaceutical development is a risky business. Investors want quick answers; each step of the process is time consuming and often dependent on factors beyond your control. You need to streamline development and keep up the momentum, but you don’t have the manpower?  Let PharmOcu help you.

We will help you find the most appropriate site(s), set up, audit, monitor, and follow up with the reporting process.  Study personnel are more responsive when they feel connected and accountable to you. We will be on site as much as necessary and monitor each step of the process via phone or E-mail to keep the study moving as efficiently and quickly as possible.

We represent you as an extension of your company in whatever capacity is needed, allowing your full-time personnel to focus on what they do best. We work with your team through constant communication to keep things moving in the right track, so your company can meet those all-important timelines and milestones.

Strategic Planning

Let us develop a customized, streamlined plan to get you quickly through clinical proof of concept quickly and cost effectively, and efficiently manage your program and timelines.

Pharmacology & Toxicology

Support services for your project including: Animal Disease Models, Drug Delivery/Pharmacokinetics, Irritation Screening/Formulation/Dose Selection, GLP Toxicology study placement and support.

CMC/Formulation Development

Ophthalmic Formulation Development, Device/Drug Release Studies, Clinical Manufacturing placement and support.


Regulatory Support Strategy/Planning, Pre-IND support/briefing book, IND Preparation.

Regulatory Support