D
darkafar
TS clause 7.6.3.1 states the requirements of an organization’s internal laboratory.
TS clause 1.2 states, “The only permitted exclusions for this Technical Specification relate to 7.3 where the organization is not responsible for product design and development.”
Clause 7.6.3.1 is not a sub-clause of 7.3, so I thought that TS requires an organization to have an internal laboratory, loud and clear.
Then I read clause 7.6.2, which states, “Records of the calibration/verification activity……shall include….an assessment of the impact of out-of-specification condition.”
By the clause 1.2 rule, this is a requirement. But we have practical difficulty, what if there is no out-of-specification happening during calibration? So I think what clause 7.6.2 actually means is that we should assess the impact of out-of-specification if out-of-specification situation happens.
Back to clause 7.6.3.1, imagine we are a very small factory. Our only process is stamping metal plate. We use caliper to measure the dimensions before and after the stamping. We send our caliper to a qualified external laboratory for calibration periodically. Why do I need an internal laboratory?
So I begin to think that internal laboratory is not a requirement, but an option. The intent of TS clause 7.6.3 is that we need to have laboratory, internal or external, to guarantee measurement traceability. But we don’t have to have both.
What do you think?
TS clause 1.2 states, “The only permitted exclusions for this Technical Specification relate to 7.3 where the organization is not responsible for product design and development.”
Clause 7.6.3.1 is not a sub-clause of 7.3, so I thought that TS requires an organization to have an internal laboratory, loud and clear.
Then I read clause 7.6.2, which states, “Records of the calibration/verification activity……shall include….an assessment of the impact of out-of-specification condition.”
By the clause 1.2 rule, this is a requirement. But we have practical difficulty, what if there is no out-of-specification happening during calibration? So I think what clause 7.6.2 actually means is that we should assess the impact of out-of-specification if out-of-specification situation happens.
Back to clause 7.6.3.1, imagine we are a very small factory. Our only process is stamping metal plate. We use caliper to measure the dimensions before and after the stamping. We send our caliper to a qualified external laboratory for calibration periodically. Why do I need an internal laboratory?
So I begin to think that internal laboratory is not a requirement, but an option. The intent of TS clause 7.6.3 is that we need to have laboratory, internal or external, to guarantee measurement traceability. But we don’t have to have both.
What do you think?