Clinical study protocol design is a foundation of clinical trials where the complexity is striking a balance between ensuring that the conclusions drawn will be robust as well as meeting all statutory requirements for data quality, integrity and subject safety. Protocols must have clearly defined objectives/endpoints, schedule of events, scientifically sound sample size considerations, statistical analyses and meet all regulatory requirements whilst also being operationally feasible. Zifo’s expert and experienced team of protocol writers, biostatisticians and medical writers work with sponsors & clinical researchers to deliver designs across clinical trials (Phase I-IV), Epidemiology / Observational studies, registry studies as well as Real World Evidence (RWE) studies.
Our Capabilities
Our expertise spans the whole spectrum of scientific process applications, and we’re able
to draw on a huge marketplace of partnerships with science technology providers, so
whatever is needed to fix your current set-up. we’ll determine the best way forward.
Our People
Our people are our business and we invest and support their development and curiosity. We actively promote science in our daily work and over 90% of people in Zifo have a scientific background – meaning we speak & understand the language of science
Glocal
We have a GLOCAL (global & local) presence – meaning we engage with you in your language and time zone but leverage a global delivery support model to remain cost-effective, scalable and very reactive
Focus
We focus on science and scientific process applications and informatics. This means we can provide expertise and domain knowledge without compromising quality, technical and service delivery excellence
Partnerships
Our huge marketplace of partnerships with science technology and informatics platform providers means you can rely on Zifo to be agnostic and advise on strategy, plan & deliver projects, and validate and maintain your scientific informatics environments
