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REGISTRATION PROCEDURES FOR TL 9000
We've
made the process of registering for TL 9000 remarkably easy.
There are eight steps for you to follow
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Step
1
Scope
Accelerate
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Accelerate will prepare implementation plan and detailed schedule.
+ Accelerate will determine the scope of the registration and
identify the relevant product category and applicable metrics.
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Step
2
Accelerate
with Quest
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As part of the TL 9000 registration process, companies must
first register with the quest forum administrator (ASQ) as a
candidate for TL 9000.
+ Accelerate will provide assistance in registration.
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Step
3
Accelerate
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+ Accelerate do gap assessment and will help to develop and implement
a documented quality management system so that it meets or exceeds
the TL 9000 requirements.
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Step
4
Accelerate
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+ Accelerate will Train and certified Internal Auditors, Executive
Management, and Employees, to conduct Internal Audits to comply
with the TL 9000 requirements.
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Step
5
Accelerate
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+ Accelerate will make arrangement with TL 9000 registrar for registration
activities.
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Step
6
Accelerate
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+ Accelerate will help to collect 3 months data, as before being
audited, a company must prove that they have submitted a minimum
of three months of metric data to the quest forum administrator.
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Step
7
Accelerate
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Registrar to conducts an on-site audit in accordance with the
selected scope and metrics that clients have prepared while
working with Accelerate.
+ Accelerate will also support on-site audit.
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Step
8
Accelerate
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On successful completion of the audit, a TL 9000 certificate
of registration is issued.
Accelerate will support any support that client may need for
maintenance of TL 9000 certification.
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Benefits
of Registration |
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When
you become registered to TL 9000,
you'll experience a wide range of benefits including:
+ Faster, better
and more cost-effective services for your customers.
+ Increased customer satisfaction.
+ Increased competitiveness.
+ Higher reliability of services.
+ Improved employee motivation.
+ Wider market opportunities.
+ Increased profits.
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We have 100% success
rate and our clients have passed in first attempt at Certification.
Our current US operations are in California (San Jose, Oakland,
Sacramento, San Francisco, San Diego, Los Angeles, Irvine), CA,
Alabama, AL, Alaska, AK, Arizona, AZ, Arkansas, AR, Colorado, CO,
Connecticut, CT, Delaware, DE, Florida, FL, Georgia, GA, Hawaii, HI,
Idaho, ID, Illinois, IL, Indiana, IN, Iowa, IA, Kansas, KS,
Kentucky, KY, Louisiana, LA, Maine, ME, Maryland, MD, Massachusetts,
MA, Michigan, MI, Minnesota, MN, Mississippi, MS, Missouri, MO,
Montana, MT, Nebraska, NE, Nevada, NV, New Hampshire, NW, New
Jersey, NJ, New Mexico, NM, New York, NY, North Carolina, NC, North
Dakota, ND, Ohio, OH, Oklahoma, OK, Oregon, OR, Pennsylvania, PA,
Rhode Island, RI, South Carolina, SC, South Dakota, SD, Tennessee,
TN, Texas, TX, Utah, UT, Vermont, VT, Virginia, VA, Washington, WA,
West Virginia, WV, Wisconsin, WI, and Wyoming, WY. With additional
operations in Puerto Rico.
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Guaranteed Certification, Consulting, Training 60-90 days for, ISO 9000, ISO
9001, ISO 14000, ISO 14001, AS 9100, OSHAS 18001, CE Mark, QS 9000, HACCP, ISO
13485, ISO 13488, ISO 16949, ISO 17025, TL 9000, TickIT, Quality, Environment,
Aerospace, calibration, Calibration Lab, ISO9000, ISO9001, ISO14000, ISO14001,
AS9100, OSHAS18001, QS9000, ISO13485, ISO13488, ISO16949, ISO/TS16949, ISO17025,
QS9000, TL9000, fda/cgmp, ISO documentation, ISO templates, standard, standards,
consultant, consultants, software, medical, medical device, quality, quality
system, telecommunication, aerospace, automotive, environment, environmental,
internal audit, lead auditor training, internal auditor training, internal
auditor course, supplier audit, acquisition audit, fda audit, cgmp augmp audit
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