
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
Digital Research Associate an EDC Tool
- Disease Registries
- Product Registries
- Real World Data Projects for Industry & Regulatory Bodies
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