Case Study: Structure, Function, Roles and Responsibilities for a Small Cap Medical Device Company
i3 Consult Case Study: Structure, Function, Roles and Responsibilities for a Small Cap Medical Device Company
The Challenges: For a
fast-growing medical device company having a global presence, there are
challenges both internal and external to the organization. Being responsive to
the regulatory, quality and safety issues, across multiple global markets can
be overwhelming to the executives of a small cap medical device company.
Internally medical device company executives are held accountable to reach
certain milestones set by Director of the Board (e.g. study completion,
licensing approval in key markets, publication of proof of concept data, sales
turnover targets, to name just a few) and/or are tasked to deal with
company-wide issues which may be either technical, regulatory, or business
related. Outsourcing to a consultant with vertical knowledge in a specific
functional area is a standard approach in systematically trying to meet the
milestones set or deal with the issues faced. Often however, faced with the
challenges of trying to integrate this consultancy-based decision making, using
the so-called compartmentalized approach, results in milestone shortfalls,
critical success issues being only partly resolved or remaining unresolved,
protracted timelines, and overspending of the corporate budget.
An Optimal Strategy: A small cap
medical device company needs to have its organizational structure, functional
roles and a comprehensive set of SOPs in place developed from their regulatory
strategy and quality management system. Their regulatory strategy and quality
management system can be developed from a cross-functional structure of their
organization which would co-ordinate the functional area talent focused on
sharing the 'Bigger Picture' of long term corporate goals. This approach of
tying in structure, functional roles and SOPs with regulatory strategy and
quality management systems has repeatedly proven effective in putting medical
device companies on the 'fast track' for cost and risk reduction as well as
championing the competitive advantage.
Action to be Taken: It is
proposed to the small cap medical device company, in all three areas of
structure, function and responsibilities of its organization, development and
deployment of an appropriate regulatory strategy, the most efficient and
compliant quality management system, and then to aggressively execute these
actions needed to demonstrate product efficacy and safety under a corrective
feedback system. Specific structures, functions and responsibilities for middle
to executive management levels are needed to ensure that there is a seamless
work flow in and around the components of the organizational structure shown (Figure
1).
Figure 1: Organizational
Structure of a Medical Device Company
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