Innovative client-centric
account management system for a complete 360° management
of clients’ requirements
Translation of clients’
requirements into practical project plans–feasibility
and project proposals
Regulatory support
services through resourceful channel of professionals
Assiduous planning,
execution and tracking of various stages of projects
One-stop compilation and
dispatch cell delivering meticulously arranged ICH
compliant study reports
Strong, insightful and updated backbone of trained pharmacokinetic personnel
Electronic archiving services transforming large clinical study data into compact digital forms
Experience:
Had been the helm of all
early phase studies since Lambda’s inception
Developed long-term
business relationship with all our clients
More than 95% success rate
in finding solutions to clients’ requirements
Effectively managed the
execution of projects with distinctive requirements, for e.g.,
elderly population studies, large postmenopausal
population studies, studies involving multiple
analytics, urgent studies aiming at first-to-file
opportunity, etc.
Huge pool of experience
with studies aimed at submission to different agencies
Services:
Client-specific account
management
Meticulously planned and
systemized caretaking of your projects
Pharmacokinetic support at
every stage
Organized tools for
planning, tracking and coordination
Supported by sophisticated
programs like WinNonlin® and SAS®
Why us?
Effective levels of
communication with sponsor
Rapid turn-around-time for
final reports as per ICH E3 backed-up by well designed
infrastructure
Latest in technology and
well-proven data management services
Quality documentation
within competitive time-frame
Customized solutions to
all your needs in clinical research
Lambda Therapeutic Research Ltd. A CRO for Clinical Research, Clinical Trials, Medical Writing, Bioanalytical, Bioequivalence and Pharmacovigilance services. India (Ahmedabad - Mumbai), Poland (Warsaw), USA