Expediting regulatory submissions with biometrics resourcing

The time and cost rigors of bringing a drug to market constantly demand optimization. Read More

Overcoming complexities of global clinical data management

Today, 60% of clinical trials data comes from external and non-EDC sources, making data collection, ingestion, and analysis m... Read More

Dynamic data visualization for smarter and leaner clinical trials

With the increasing complexity of clinical trials, digital data sources are now routinely leveraged for more in-depth safety ... Read More

Simplifying clinical risk and quality management

ICH-GCP E6R2 clearly defines the prerequisites of risk and quality management impacting patient safety and the integrity of d... Read More

Starting stronger with early evidence generation

Several critical factors including poor scientific planning, overlooking critical safety signals, and erroneous estimation of... Read More

Risk-based approaches to managing your clinical data

With the goal of making clinical trials more and more patient-centric, decentralization has introduced newer complexities in ... Read More

Readying your digital infrastructure for the future

As the clinical trial journey progresses, a key issue that emerging biotechs deal with, is scattered data due to multiple par... Read More

MetaVate: Metadata-driven automation for clinical data flow and transparency

Download our brochure to learn how MetaVate supports any source to any target relational data transformation. Read More

Visualizing the patient journey

Oncology clinical trials have multitudes of challenges and given the duration and complexity, understanding, and visualizing ... Read More

Accelerating early stage development with IDEAS

Download our brochure to learn how IDEAS enables biotechs accelerate early-stage development Read More