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SCPI Commitment

Most of us are very conscious about the components of the food we eat.  We shop carefully, watching calories, fat content, and good cholesterol versus bad cholesterol.  We do this for the health of our children and future generations.  We are able to do this because of US FDA NLEA (Nutrition Labeling and Education) requirements.

Not only do we care about what is in our food, we also care about how it was produced.  Is it organic?  Is it green?  Is it good for the rain forest?  Were people exploited to produce it?  Were the animals treated well?  For many of these questions we can find answers by looking for certification stamps on our food packages. 

Do we do this for our medicines?  Is there any legislation comparable to the US FDA NLEA requirements that compel drug companies to tell us what is in our medicines?  Is there a certification stamp that can assure consumers that human DNA and cellular debris is not part of the vaccine or drug they are using?  How can we know that another human was not exploited to develop our medicine?

Over the past decade the use of aborted fetal material has slowly, almost imperceptibly, seeped into and become routine at many stages of drug discovery, development and commercialization, to the point where aborted fetal material is now being used to discover new food additives and flavor enhancers.  How did this happen?  Why aren’t we aware of this?