Medical Affairs
The lack of clear regulatory requirements for a medical
affairs department, combined with the evolving state of the
life science industry, has led to a number of issues for
medical device and pharmaceutical companies to consider when
and where establishing and maintaining a medical affairs
department.
The role of our medical affairs
specialists is to ensure building adapted capacities and
meeting local and corporate requirements in a the era of
globalized entities , to assist your company operations in
your emerging markets within our expanding coverage zone.
Our staff closely interacts with physicians and other
healthcare professionals whom are involved in research or
already use your products , handling various thematics such as
: research grants issues , medical communication , off label
usage , publications , safety informations and
providing/assisting in an independent targetted medical
education.
The KOL management using services of Advisory Boards
It is now accepted that becoming a drug depends closely on
efforts deployed by its holder to educate prescribers on the
various problems encountered in several contexts: coverage
insurance by CNAM, comparability with competitors of the same
class and keeping them informed along with considering their
advice about current and future patterns of innovation for
clinical development.
The thematic advisory boards
that can be tools of conflict resolution, retention, and
exploratory marketing methods allow a collection and a
relevant exchange with KOLs.
Our team reflects on the
problem with the Product Manager / Medical Manager client and
ensures the organisation and logistics tracking (invitation,
local, writing PV of the advisory board, translation if
required).