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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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Planning

Planning will be executed at all stages with customized services as per client's request. It will deal in drug discovery, pre-clinical testing, clinical trials and post market drug safety and life cycle management.

Clinical development will be the first phase for product development. At this stage, poor clinical development analysis can withhold the information for the future prospect of the trial. GAP provides product profile with interim analysis. Taking into account the critical hurdles like clinical trial design, patient pool availability, feasibility, ever changing circumstances with changing regulatory requirement, GAP meets the set benchmarks.

Contact us for more information.