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Peer review
paper published
by GAP

Medical writing,
Clinical Expertise,
Technical Development
is our core
competency

Data Safety
Monitoring Board
(DSMB)

DSMB

Clinical
Events
Committee

CEC

Safety
Assessment
Committees

SAC

Message
from
the CEO

President
and
Co-founder

Our
Service
Card

Business
Card

Automated
Remote Data Manage
QC and Medical
Monitoring
Service

Business
Card

We wrote
the book
On
GPV & E

Pharmacovigilance
is
What We Do.

We wrote
the book
On
Immuno-Oncology

Oncology-Clinical
Devlopment
is
What We Do.

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Site Management

Site Management is a comprehensive relationship management with investigators and Clinical Research Coordinator (CRC) team along with management of all site documents and logs. GAP provides facilities like on-line site training and certification, study education and Good Clinical Practices (GCP) training to speed Institutional Review Board (IRB) submission and approval, and to facilitate patient selection, enrollment and randomization. We appoint highly qualified CRC at each study to assist and support the investigators and site staff with all study related activities, ensuring compliance with FDA, local regulatory and International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH)-GCP guidelines and an efficient completion of assigned duties.

Contact us for more information.