BUSINESS

Clinical Operation

Overall project and site management which includes developing protocol & CRF, IND/IRB submission & approval etc.

VIEW

Regulatory Affairs

Pre-IND meeting and overall MFDS related work including IND/IRB Dossier preparation, submission and approval.

VIEW

DM/STAT

Study design, sample size calculation and paper/electronic CRF development and Data Management & Statistical Analysis.

VIEW

QA/QC

Quality control and quality assurance work based on SOP development, GCP and related regulations.

VIEW

Consulting

Overall consulting which include clinical trials and registration of pharmaceutical products, medical devices, health functional foods, and cosmetics.

VIEW

“ From bench To launch! - PharmaCRO

COMPANY

PharmaCRO looks beyond clinical trials and aims to grow together with our clients based on scientific specialties,
professionalism and competitive strengths.

CUSTOMER