Capabilities & Products - Metrics Research

Solutions for Bio/ Pharmaceuticals, Research Institutes, Health Regulators

Clinical Research

Research Proposals, Protocols, Feasibility, Regulatory Affairs, Clinical Operations, Data Management, IRB, Trainings, Expert Reports, Quality Assurance:

Phase I to III & Phase-IV (PMS) Clinical Studies
Epidemiology Projects

BA/BE Studies

Bioavailability & Bio-equivalence Projects

Pre-Clinical Study Projects

Bioavailability & Bio-equivalence Projects

Digital Research Associate an EDC Tool

Disease Registries
Product Registries
Real World Data Projects for Industry & Regulatory Bodies

Pharmacovigilance

AE/ SAE Reporting
Risk Management Plans

Metrics Institute For Clinical Research Science

CCRP Course – partnered with Kriger Research Center International – Canada
Workshops – partnered with Kriger Research Center International – Canada
GCP & Bioethics in Clinical Practice

Strategic Support to Bio/ Pharmaceutical Industries

Local / International Regulatory Aspects

Dossier Compilation & Filing (CTDs & eCTDs)
Regulatory Authority Query Handling

Novel Medical Strategies

Market Research Insights
Marketing Authorizations
Market Launch Support