RARE DISEASE CRO SERVICES
RARE DISEASE CLINICAL TRIAL OUTSOURCING SUPPORT
Work with a CRO that has Rare Expertise
At PharPoint, we understand the unique challenges that come with studying small patient populations, navigating complex regulatory pathways, and ensuring patient-centric trial design. As a team that offers rare disease CRO services, PharPoint has supported a wide range of trials. Our experience also includes providing biometrics support according to industry best timelines.
250+
Rare disease trials supported across all services
10+
Regulatory submissions supported
TESTIMONIAL
What Our Clients Have to Say
CLIENT:
Small rare disease company
SERVICES PROVIDED:
Clinical operations, data management, biostatistics
“…we knew we needed a CRO who was vested in our collective success, a true and trusted partner who would be flexible, attentive and engaged in achieving our end goal. We also needed to work with an experienced, competent team who we could rely on and an approach to the contracting that offered value, without compromising quality. In our partnership with PharPoint we have found all of this and more.“
General Manager
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ABOUT PHARPOINT
Explore PharPoint’s Rare Disease CRO Services
PharPoint Research is a client-focused, US-based contract research organization that helps sponsors meet their clinical trial goals.
Our rare disease CRO services include:
Confidently make informed decisions and advance your product along the development pathway with support from our regulatory, clinical, medical, and biometrics consultants.
We work to ensure study excellence and transparent collaboration between CRO, site, and Sponsor. Our teams are highly accessible and work closely to build excellent site relationships that streamline communications, encourage efficiency, and ensure compliance.
Receive high quality support and deliverables from our data management and biostatistics teams – all according to our industry-best biometrics timelines.
PharPoint’s medical writing team can provide you with accurate, clear, and concise clinical trial documents.
Concerned your current clinical trial outsourcing partner is placing your study on the backburner? PharPoint’s flexible support includes clinical trial rescue services as well as CRO oversight.
What Our Clients and Partners Say About Working with PharPoint
“My experience working with PharPoint has been a pleasure. They have taken ownership of our clinical trial since day one. I truly feel that we work as one team.”
Sr. Director, Clinical Operations, Biopharmaceutical Client
“PharPoint has been helpful in study rescues, high priority pivotal studies locked and delivered faster than any other CRO I have worked with in my experience. Not only was the study delivered within budget and early, it was a quality deliverable.”
VP Clinical Operations, Biotechnology client
“I can highly recommend partnering with PharPoint. Not only were documents provided to our site in a timely manner, communication with all parties from the CRA to the project managers has been excellent. Our site has not had any trouble with reaching our PharPoint contacts when in need of assistance, either by email or phone. When follow up is required, I can count on it being addressed quickly and accurately.”
Site coordinator, study partner
Reach Out to an Experienced Rare Disease CRO Team