Our services

Our Services

Genpro offers full array of clinical data, statistical, regulatory and submission services through our very experienced team in USA and India. We offer the full spectrum of services to help people work better. Everything from creating standards of excellence to helping your people to work in more effective ways.

CLINICAL DATA MANAGEMENT

Genpro offers an experienced team of clinical data managers and clinical data coordinators who comes with a life science background. They are trained in ICH/GCP as well as CFR PART 11 guidelines. Genpro has extensive experience in various EDC tools and provides EDC setup services to different phases of clinical trials.

STATISTICAL PROGRAMMING

We deliver consulting services in the areas of Biostatistics, SAS programming, FDA interactions and Regulatory interactions. At Genpro we have an experienced and dedicated team of developers with detailed knowledge of all phases across the drug development spectrum.

BIOSTATISTICS

GenPro offers expert consulting services on complex statistical issues encountered during study design or analysis. We provide guidance in incorporating and analysing the effectiveness of statistical methodologies in clinical trials with a great deal of expertise in adaptive designs and Bayesian analysis.

BIG DATA ANALYTICS

Genpro provides clinical data visualization dashboards and drill down reports to help sponsors to monitor their clinical and safety data. We can provide sponsors with web based dashboards to monitor their clinical data including tabular and graphical reports from a single database or across multiple databases.

STRATEGIC CONSULTING

Genpro provides strategic consulting services in regulatory submissions, data submissions and early stage studies.Our expert pool of statisticians, regulatory experts and Submission specialists will help our clients at every stage of the trial. We will support you through the FDA interactions and data monitoring committee support.

MEDICAL WRITING

Genpro has a pool of medical writers and medical coders with several years of experience across various therapeutic areas. Our consultants are trained on ICH E3 guidelines and work very closely with our US team of statisticians and medical writers.

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