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Development Platform

General Pharmacology study
Acute toxicity and repeated
dose toxicity study
Genetic toxicity study
Reproductive toxicity
Special safety study
Toxicokinetic study
Candidate compound
optimization
Structure elucidation
API process research
Small and pilot sample
preparation
Reference standard
preparation
API container closure
system selection
Preformulation study
Formulation and
process study
Pilot sample preparation
Packaging material and
container selection
Communicate with PFDA and SFDA
Write and submit application data
Prepare for the on-site inspection
Participate in Evaluation defense
Quality study
Quality specification drafting
Stability study
Sample release test
Biological analysis method development and validation
Pharmacokinetic study
Drug absorption, distribution
and excretion study
Drug metabolism research
Pharmacodynamic
evaluation in vitro
Pharmacodynamic
evaluation in vivo
Pharmacological
mechanism study
Zhangjiang Hi-Tech Park
State-level Toxicological
Research Institute
Pharma-ceutical Analysis
Toxicology
Medicinal Chemistry
Process Chemistry
Pharma- ceutical Preparation
IND Filling
Pharma-cology
Pharma-cokinetics
Pre-Clinical Development Management
Subcontract
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