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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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Drug safety & Pharmacovigilance

GAP has a team of experts in all associated areas of Pharmacovigilance and drug safety. With ever changing regulations, drug safety is an ever evolving sector of biopharmaceutical companies. We serve our clients by creating a safety profile of the drug or a device. Our services includes, but is not limited to: Case management, QPPV services, risk management, medical review, signal detection, audit and inspection services, aggregate reporting, as well as narrative writing. We will engage from simple reporting of case to preparation of expert report of the drug profile. This is not short-lived, but will be followed through the life cycle of the product. We are capable to manage the large pool of data and systematically analyze the data as needed.

We provide the following services:

Related Links:-

Clinical Development, Regulatory, Due-Diligence, Medical Monitoring

Contact us for more information.