CNS CRO SERVICES
CNS CLINICAL TRIAL OUTSOURCING SUPPORT
A CRO with Extensive Neurology Clinical Trial Experience
PharPoint has provided CNS 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:
- Schizophrenia
- Pain
- Parkinson’s Disease
- Multiple Sclerosis
- Insomnia
- Major Depressive Disorder
- Alzheimer’s Disease
- Substance Use Related Indications
- Seizures
- Fever
- Rare indications
40+
CNS indications supported
175+
CNS trials supported across all services
10+
regulatory submissions supported
A CNS EXPERIENCED CRO
How PharPoint Successfully Supports CNS Clinical Trials
Facilitating the flow of study information
We understand that neurology studies are often highly complex, including both vast amounts of data and, very frequently, a large number of specialized study team partners that must be kept on track.
The PharPoint team works diligently to prioritize proper planning, onboarding, and ongoing management and communication – keeping sponsors in the loop and remaining nimble and able to react to a changing environment, when needed.
Overcoming challenges unique to neurological pathologies and assessments
We help sponsors dig into their study details and ensure an effective, seamless-as-possible trial.
PharPoint’s experts can bring valuable insight to a study, partnering a deep background in clinical research operations with an understanding of neurological conditions, clinical assessments, and IP administration.
Get study results faster
With strategic early planning and collaboration, efficient study processes, and a seasoned study team, PharPoint helps sponsors meet rapid study timelines. For more information about average biometrics CRO timelines, the standard timelines PharPoint provides, and how our team can help you achieve study goals faster, meet with our team.
EXPLORE CNS RELATED RESOURCES
Supporting Schizophrenia Clinical Trials: Keys to a Successful Study
What should sponsors take into consideration when planning a schizophrenia clinical trial & download PharPoint's experience overview.
Experience Overview: Supporting Alzheimer’s Disease Clinical Trials
Looking for a CRO to support an upcoming Alzheimer's disease clinical trial? PharPoint’s experts work as an extension of your team to strategically plan, execute, and analyze Phase 1 – Phase 4 Alzheimer's disease clinical trials.
Alzheimer’s Disease & Decentralized Clinical Trials
Should your Alzheimer's disease clinical trial be decentralized or include virtual aspects? In this article, we discuss potential benefits.
ABOUT PHARPOINT
Explore PharPoint’s CNS CRO Services
PharPoint Research is a client-focused, US-based contract research organization that helps sponsors meet their clinical trial goals.
Our CNS 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
“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
Reach Out to an Experienced CNS CRO Team