Concept 2 Clinic will:
technology assessments and due diligence for in-license
opportunities or repositioning;
experts for presentations, discussions and interactions with
business, clinical and regulatory plans and budgets to support
clinical protocols, site selection and study management;
toxicology, animal modeling, and safety pharmacology pre-clinical
capacity or capability for formulation development or technology
transfer; supply team members to complement existing
organizations to execute development plans;
on clinical and regulatory strategies and provide
consultation on specific elements of a development program; and/or
provide expertise to resolve technical issues;
and Quality assessment of manufacturing, analytical and support
services (toxicology, data management, CMO, CRO etc) facilities;
additional capacity or capability to your organization to meet
global business development and enhance financial partnering
government grant applications
general list of our services is listed below.
Should you require additional information, please do not hesitate
to contact us.
product development strategy for fund raising and government grant
application with emphasis on appropriate business plans, market research
and technical assessment.
due diligence and assess technology and from a scientific and business
expert opinions and strategic advice on pre-clinical studies, submission
enabling plans and execution.
audit and manage vendors and service providers and be accountable for
client timelines, budgets and technical support.
Regulatory / Quality
documents for submission and interact with regulatory agencies on behalf
clinical protocols and select appropriate sites for clinical trials,
management and monitoring of studies.