Bioequivalence studies
TehranChemie is providing bioequivalence and pharma cokinetic studies through cooperation and partnerships.These studies are in compliance with current good clinical practice(cGCP),current good laboratory practice(cGLP),and other applicable guidelines and regulations.The full Bioequivalence study service covers:
Wide selection of appropriate study designs
The writing of study protocol
Designing of case report forms (CRF)
Management of Independent Ethics Committee reviews
Selection and care for subjects
Bioassay of drug/metabolite
Pharmacokinetic and statistical data evaluation
Reporting of study results and archiving of all trial-related data
Medical
- Writing patient leaflet for new products based on the scientific references
- Preparing medical and scientific data in order to support the sales & marketing teams with up to date information
- Preparing materials such as posters and patient information booklets
- Answering patients and healthcare professionals’questions about company’sproducts and scientific subjects are answered by medical team members
- Team work and collaborating with marketing departments