Pharmaceutical Consulting Services
You may be a Pharmaceutical Company, a Virtual Company, a Research unit or Academia who could well benefit from my extensive portfolio of services based on 30 years experience of early drug development.
http://www.peterdewlandconsulting.com
Regulatory
- Clinical Overview
- Expert Reports
- Representation at meetings with Competent Authority (CA)
- Handling questions from CA
Training
- GCP
- Therapeutic
- Pharmaceutical Medicine
- Clinical Science
Clinical Pharmacology
- Feasibility
- Advice regarding MHRA inspections
- Advice on First in Human (FIH) studies
- Advice on EAG (High risk) molecules
- Biologicals
- Vaccines
- Pharmacodynamics and surrogate markers
- Selection of CRO and Phase I unit and placing of studies
- Ethics Committee submissions
- CTA submissions
- Protocol design and writing
- DSMBs
- Bioavailability and bioequivalence
- Interaction studies
- Toxicology review
- 24 hour medical cover
- Report review
- Access to
- Clinical Writing
- CRAs
- Data Management and statistics
- Pharmacokinetics