Mayfair
has an excellent team of professionals who
are rich in experience of conducting bioavailability
and bioequivalence studies coupled with
an excellent infrastructure of Clinical
and Bioanalytical sections to support various
kinds of studies. We can conduct:
Bioavailability/
Bioequivalence studies on Conventional
release or modified release formulations
Studies under fasting
or fed conditions
We help our valuable
clients in
The protocol
and the Informed Consent Document preparation,
The study design,
planning & execution,
Bioanalytical
data generation,
Statistical
analysis and
Writing the
entire study report.
All our protocols and
the informed consent documents are approved
by Independent Ethics Committee (IEC) following
ICH-GCP guidelines for international acceptance
before the initiation of the study.
The implementation of
our SOPs and our continuous QA monitoring
helps us to conduct the studies as per the
GCP and the GLP norms and thus meet the
international as well as the local regulatory
requirements.
Our large pool of volunteers
helps us to conduct the study faster.
State-of-the-art clinical
facilities including:
Volunteer housing
with 32 beds
Physician’s
room equipped with ECG, Mercury Sphygmomanometer
Emergency room
Phlebotomy room
Volunteer recreation
and audio-video entertainment room
Volunteer’s
Dining Room and Wash Rooms
Study Monitor’s
room and
Utilities room consisting
of cooling centrifuge and deep freezer
for plasma sample storage.
Zymark’s Solid
Phase extraction and evaporation unit
for purification of plasma samples
Liquid-liquid Plasma
extraction procedures.
We develop the
sensitive bioanalytical method, which is
validated as per the international guidelines
and we ensure our clients of faster and
accurate analysis and in a cost-effective
manner. This is just another way in which
we help our clients to take the right decisions
faster and at the same time being cost-effective.
