DERMATOLOGY CRO SERVICES
DERMATOLOGY CLINICAL TRIAL OUTSOURCING SUPPORT
PharPoint has provided dermatology CRO support for sponsors conducting clinical trials across multiple indications. Our experience also includes providing biometrics support according to industry best timelines.
PHARPOINT’S EXPERIENCE INCLUDES:
A DERMATOLOGY CRO CASE STUDY
Phase 2 Full-service support Dermatology
A sponsor selected PharPoint to provide full-service CRO support for a Phase 2 dermatology study that involved two investigative sites.
PharPoint worked closely with the sponsor, investigative sites, and specialty study vendors. The trial enrolled rapidly, completing well ahead of schedule.
The PharPoint team moved quickly to achieve a rapid database lock and delivery of results.
Ultimately, we were able to deliver a locked database two months before the study had originally planned to complete enrollment.
EXPLORE RELATED RESOURCES
ABOUT PHARPOINT
PharPoint Research is a client-focused, US-based contract research organization that helps sponsors meet their clinical trial goals.
Our Dermatology 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.
“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
“In advance I would say that our experience with PharPoint has been very positive. As a smaller company, I was concerned we would get lost and deprioritized with one of the larger CROs, and in fact that had been the case with a prior CRO who we had contracted for our study. We went out to bid for a new CRO and the PharPoint team came out of nowhere with an excellent pitch. Not knowing them as well as larger competitors we were cautious, but they delivered thoughtful responses and solutions at every stage. We decided to move forward with them and I can honestly say I have never had any feelings of buyer’s remorse or any observed any bait and switch – they remained as committed to our mission over the period we worked with them as they were in the initial meetings.”
US General Manager, Pharmaceutical 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