Consumers are always
seeking a quality product – no matter what industry the product is intended
for. However, the complexities of most products today bring about an inherent
problem: one industry does not necessarily control production up and down the
chain. Thus, it is generally difficult to ensure quality control beyond one’s
own company. This lack of control could be unnerving, if not for an unexpected,
guiding principle: fault.
This principle of accountability
holds true within the realm of Clinical
Research Organizations (CROs). Liability drives companies to create better
products, and fault is an ever-present motivator. In the case of CROs, these
organizations find themselves in a delicate position of having to be cautious
about whom they are dealing with in both upward and downward directions:
medical sites, clinical research assistants, sponsors and subcontractors.
Every step of the way, your
contracts must stipulate that the quality of work is guaranteed, and allocating fault
and responsibility is a key element to that.
No matter who is involved in the process, though, there must be assurance
that quality is assured, starting at the top and running straight to the
bottom.
My yard, like many yards, is
inhabited by a number of squirrels who assume they belong on my property. My
dog will bark, informing them that this is, in fact, not their yard. While an
audible yap is not necessarily a powerful deterrent to the squirrels and their
trespasses, the constant threat and physical presence of the dog keeps them on
their toes. People in contracting relationships can think of the dog’s bark as
“fault.” While the persistent threat looms, there is always the possibility of
greater danger – such as a loose dog that can chase you.
The liability associated with a
bad drug reaction – or even worse, introducing a dangerous or deadly drug to
market – is huge. To prevent this from happening, CROs must have clearly
defined guidelines and expectations for all the organizations and individuals
involved. This runs deeper than being a blueprint for the “blame game.” This
means establishing a method to ensure data integrity, which, in the realm of
CROs, ultimately translates to public safety and health. CROs are not just
trying to indemnify themselves, but they are making sure that every step along
the way preserves the highest quality work.
The world of life science is a
challenging and competitive ecosystem of tests and trials. Fortunately, there
are some governing principles that help ensure the safety of those within it.
For CROs, they can feel assured that the threat of fault will ensure that the
best product possible can come from the system, and the greatest good can be
done so that the consumer can have the maximum benefit.
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