Vigilance is our key for patient safety. Patient safety is our primary and main objective!
Statistics & Data Analysis
We choose the right statistical tool and computational model to analyse your data.
We streamline clinical operations to provide efficacious solutions for complex projects.
MD Pharma Consulting Group supports our clients' clinical research writing needs for:
- Clinical study protocols.
- Informed consents.
- Medical coding conventions.
- Safety module specifications.
- Medical management and safety plans.
- White papers.
- Investigator brochures.
- Serious adverse event narratives.
- Investigational New Drug (IND) safety reports.
- Data Safety and Monitoring Board (DSMB) summaries/updates, etc.
MD Pharma Consulting Group supports our clients' biomedical research scientific writing needs during the preclinical drug and medical device development phase. We provide extensive literature review that will validate our clients' lab study hypothesis. We can help with the experimental design and choose the right biomedical lab technologies suitable for our clients' lab study.
MD Pharma Consulting Group supports our clients' regulatory affairs writing needs. We have open communication channels with the regulators, know the required regulatory documents, and know when and how to submit them.