The turning point that transforms your trials into triumphs.
PiVOT
PiVOT is the largest and fastest-growing Philippine Contract Research Organization. It advances the field of clinical research in the local health industry through innovations in drug safety surveillance, clinical trial monitoring, and clinical trial support services.
The PiVOTal Difference
PiVOT starts with ‘pi’, a value as precise and limitless as their capability to help clients, enabling them to execute clinical research with validity, optimization, and transparency. Our Network Partner's expertise with site management organization and clinical trial support services constitutes the turning point that transforms your trials into triumphs.
PiVOT By The Numbers
23
Sites
16
Studies
40,000+
Participants Recruited
Drug and Device Trial Management
PiVOT manages Phase I to IV trials for drugs, biologics, and devices, focusing on proof of concept or small-scale studies. Services encompass protocol development, regulatory affairs, monitoring, data management and analysis, and report writing. Ensure compliance with Data Privacy Laws, Good Clinical Practice, and relevant regulatory guidelines. PiVOT strives to support publication in peer-reviewed journals or facilitate decisions on advancing to large-scale FDA registration trials.Post Marketing Surveillance (PMS) and Real World Evidence (RWE)
PiVOT provides comprehensive support for Post Marketing Surveillance (PMS) and Real World Evidence (RWE) studies, from pre-regulatory stages to study close-out and data analysis reporting. Services ensure compliance with Data Privacy Laws, Good Clinical Practice, and relevant regulatory guidelines. They cover protocol development, monitoring, data management and analysis, and report writing for seamless execution of studies.
Other Services
PiVOT provides a comprehensive range of services to help you succeed in clinical research. Their team of experienced professionals is here to guide and support you through every step of the clinical research process, from identifying the right study design to helping you understand the results. With their expert guidance, you can be confident that you are receiving the highest quality research services available.
Site Management Organization
Medical Writing
Regulatory Affairs Assistance
Investigator-Initiated Research
Bioavailability & Bioequivalence Studies
Experienced Training Staff
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.