Clinical Trial Expertise for the Pharmaceutical and Biotech Industry
Strategic and operational clinical trial support from seasoned pharmaceutical consultants with global, multi-phase experience.
Driving Clinical Trials from Strategy to Execution
At GOT Pharmacology, we provide full-spectrum clinical trial expertise to pharmaceutical, biotech, and medical device companies. Our consultants bring decades of experience across Phases I–IV, helping sponsors design smarter trials, reduce timelines, and navigate complex regulatory landscapes with confidence. Whether you need support for a single study or an entire portfolio, we embed ourselves in your team to accelerate progress and ensure clinical excellence.
Protocol Design and Feasibility
We help sponsors develop strong, compliant clinical protocols aligned with scientific objectives and operational realities.
Our team balances innovation with regulatory expectations to ensure protocols are feasible, ethical, and set up for success.
Trial Start-Up and Site Activation
We support site selection, feasibility analysis, contract negotiation, and regulatory submissions to streamline the start-up phase.
Our consultants reduce site delays and ensure smooth activation through local expertise and proactive coordination.
Clinical Project Management
Our experienced project managers lead studies from planning through closeout with precision and accountability.
We focus on real-time issue resolution, timeline adherence, and cross-functional collaboration to keep trials on track and sponsors informed.
Vendor and CRO
Oversight
We provide strategic oversight of CROs, labs, and vendors to ensure quality, compliance, and budget control.
Our consultants act as your eyes and ears on the ground, holding partners accountable and minimizing risk to trial integrity.
Data Management and Quality Monitoring
Our experts ensure that your trial data is clean, accurate, and audit-ready.
From database build to query resolution, we implement high-quality data processes and ensure ongoing monitoring aligns with regulatory and safety standards.
Regulatory and Submission Support
We assist with regulatory strategy, correspondence, and submission packages throughout the trial lifecycle.
With experience across FDA, EMA, and other global agencies, we help you navigate the complexity with clarity and speed.
