C
crendfrey
Greetings all,
I am thanking you all now in advance for helping me through what is coming next for me. I am also begging forgiveness for the long winded questions and explanations.
The Story:
My employer in his infinite wisdom has purchased another calibration lab which effectively doubles the size of my company. (job security for me)
This company was at one time 17025 accredited by a not so reputable AB.
I was hoping to have site specific accreditation by March 2008.
No such luck.
In order to keep a very large customer, who is willing to use some of the work a rounds I seem to have pulled out of my hat, requires accreditation sooner.
They will accept scheduling for accreditation in 90 days. Full accreditation by no later than Feb. 1st.
Its not that the system is a mess, it is just there seems to be no rational system at all.:mg:
I have decided to impose our existing system on them. I feel I am unable to administer 2 different systems in now 5 states.
My first hot issue is traceable certificates for calibration standards.
All standards must be certified by State labs in order to comply with various state weights and measures regulations.
I have a state lab that I use for the original company which I trust implicitly.
For the new company to get to that lab will require a 6 hour drive time to deliver and again to pick up. Not very cost effective.
A state lab less than an hour away has a “conditional” approval through the MAP program.
Now comes the questions for a sage 17025 auditor/assessor……..
Is this acceptable? Given my time constraints, it would be most convenient if it is.
By the same token I do not want to have to do ANYTHING multiple times. I personally have a problem with the word “Conditional” however in the interest of time and cost……. Will it fly?
PS. Many more questions will be coming at you all about FDA and Pharmacopeias,(they seem to have strange definitions of uncertainty) but first things first.
I am thanking you all now in advance for helping me through what is coming next for me. I am also begging forgiveness for the long winded questions and explanations.
The Story:
My employer in his infinite wisdom has purchased another calibration lab which effectively doubles the size of my company. (job security for me)
This company was at one time 17025 accredited by a not so reputable AB.
I was hoping to have site specific accreditation by March 2008.
No such luck.
In order to keep a very large customer, who is willing to use some of the work a rounds I seem to have pulled out of my hat, requires accreditation sooner.
They will accept scheduling for accreditation in 90 days. Full accreditation by no later than Feb. 1st.
Its not that the system is a mess, it is just there seems to be no rational system at all.:mg:
I have decided to impose our existing system on them. I feel I am unable to administer 2 different systems in now 5 states.
My first hot issue is traceable certificates for calibration standards.
All standards must be certified by State labs in order to comply with various state weights and measures regulations.
I have a state lab that I use for the original company which I trust implicitly.
For the new company to get to that lab will require a 6 hour drive time to deliver and again to pick up. Not very cost effective.
A state lab less than an hour away has a “conditional” approval through the MAP program.
Now comes the questions for a sage 17025 auditor/assessor……..
Is this acceptable? Given my time constraints, it would be most convenient if it is.
By the same token I do not want to have to do ANYTHING multiple times. I personally have a problem with the word “Conditional” however in the interest of time and cost……. Will it fly?
PS. Many more questions will be coming at you all about FDA and Pharmacopeias,(they seem to have strange definitions of uncertainty) but first things first.