Welcome to PiVOT
Chasing a medical breakthrough?
Your next step could be PiVOTal.
The PiVOTal Difference
PiVOT starts with ‘pi’, a value as precise and limitless as our capability to help our clients, enabling them to execute clinical research with validity, optimization, and transparency. Our expertise with site management organization and clinical trial support services constitutes the turning point that transforms your trials into triumphs.Services
Drug and Device Trial Management
- Management of Phase I to IV trials on proof of concept or small scale trials on drugs, biologics, and devices
- Designed for publication to peer-reviewed journals or to support the decision to pursue large scale FDA registration trials
- Compliance with applicable requirements such as Data Privacy Laws, Good Clinical Practice, and applicable regulatory requirements and guidelines
- Services include protocol development, regulatory affairs services, monitoring, data management and analysis, and report writing
Post Marketing Surveillance (PMS) and Real World Evidence (RWE)
- Post Marketing Surveillance (PMS) and Real World Evidence (RWE) studies end to end support from pre-regulatory and start-up to close-out and clinical study data analysis reporting.
- Compliance with applicable requirements such as Data Privacy Laws, Good Clinical Practice, and applicable regulatory requirements and guidelines
- Services include protocol development, monitoring, data management and analysis, and report writing
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Site Management Organization (SMO)
Our SMO platform provides contract research organizations (CROs), pharmaceutical and biotechnology companies, medical device companies, and especially clinical investigation sites – our critical partners – with excellent clinical-trial-related services, including:
Get your time back and let us find the solutions you need!
GLSA’s Global Network of solutions incorporates a variety of CROs and specialty vendors to support the specific needs of your clinical trial. Our network includes full-service CROs, biometrics, site selection, patient recruitment and retention, clinical supply chain management, and more. GLSA pre-qualifies all members of our network so you can be comfortable working with quality service providers.
We connect Sponsors with the CRO that has the right experience, culture, and capabilities to execute their research protocol. We leverage our extensive experience and harness our key relationships to work for CROs. We can fill any gaps you need to support your client’s trials. GLSA takes the guesswork out of vendor selection with our industry experts and experience.
What are your challenges? Contact GLSA to learn more about how we can help you accelerate your speed to market.