I will analyze preclinical study data and prepare regulatory reports for pharma clients
PhD Pharmacist, Clinical Research Scientist and Medical Writer
About this Gig
Do you need expert preclinical data analysis and professional regulatory report writing for your pharmaceutical or biotech company?
I am Dr. Arfat Yameen, a PhD pharmacist and active clinical research scientist at Continuum Research Center (CRO) with 15+ years of academia and professional experience.
What I offer:
- - Protocol design, data collection and statistical analysis of preclinical study data for industry clients
- - Drug safety and toxicology data interpretation and reporting
- - Regulatory report preparation for DRAP, FDA, EMA, and ICH submissions
- - GCP-compliant preclinical documentation for CROs and pharmaceutical companies
- - Pharmacokinetic and pharmacodynamic data analysis
- - Dose-response analysis and efficacy reporting for industry
WHY CHOOSE ME:
- - Active scientist at Continuum Research Center (CRO)
- - Experience with GLP, ICH-GCP standards
- - Trusted by national and international pharma and biotech companies
Order now for GLP-compliant, industry-ready preclinical reports!
Service type:
Research
Language:
English
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