|
Need a Quote?
Orion is committed to making
the quoting process as comfortable as possible. We know shopping
around for a Registrar can be an unpleasant experience with pushy
sales people. Our goal and guarantee is to give you the information
you need upfront to make the best decision for your company. Call,
Email, or Fax us for a quote:
Lori Correia
Phone: 303-645-4017
Fax: 303-645-4875
Email: marketing@orion4value.com About
Orion
This website contains articles about ISO
9001, AS9100, ISO 14001, TL9000, HACCP,
ISO 13485, CE Marking for Medical Devices, the FDA's
Inspection by Accredited Persons (IAP) Program, and CAB.
It also contains articles about choosing
a registrar, the
registration process
information about our company, Orion
Registrar, and our registration
services.
You may also use our website to obtain a free quotation.
Our primary goal is to provide you with the objective information you
need to make the best choice possible in a registrar. Besides the
information here, please take us up on our offer to answer any of your
questions about quality or environmental management systems and
Orion's registration process.
Thank you for visiting,
Paul
Burck President, Orion
Registrar, Inc.
|
|
ISO 9001:2000 Client Notification
Beginning September 1, 2009 all QMS certification and recertification audits will be conducted to the ISO 9001:2008 Standard. Since all ISO 9001:2000 certificates will become invalid after November 14, 2010, all client surveillance audits conducted after October 1, 2009 must be to the ISO 9001:2008 Standard. This will help insure that most clients' certificates will not expire in November 2010 and will help our clients to avoid the cost of an additional transition surveillance audit before the November 14, 2010 expiration date of the ISO 9001:2000 Standard.
In order to be sure of transitioning to the ISO 9001:2008 standard by the deadline, Orion strongly recommends that clients have their transition audit by June 14, 2010, which is five months before the withdrawal deadline. A five month window allows 120 days for any major nonconformities to be corrected by the client, verified and closed by Orion, and 30 days for the certifier to review and certify the file. A client cannot be recommended for certification to ISO 9001:2008 with open major nonconformities.
Due to the number of clients involved in this transition, Orion strongly suggests that clients plan and schedule their transition to the ISO 9001:2008 Standard as soon as possible to avoid any backlogs during the final months prior to the deadline.
Transition to ISO 9001:2008
Orion has created its transition plan based on a joint IAF-ISO communique
on the subject.
Please click here for Orion's Transition Plan Entire
Article
ISO/FDIS 9001:2008 Overview
View
Entire
Article to review changes
to the ISO 9001 Standard.
Purchase
ISO 9001:2008 Standard
http://www.asq.org/iso9001/
Orion Earns ISO 17021 Accreditation
Before Deadline
Orion Registrar is pleased to announce that we have earned
ISO 17021 accreditation from both ANAB, the U.S. accreditation body and RvA, the Dutch accreditation body.
Entire
Article
Orion Earns e-Stewards®Accreditation
Orion Registrar, Inc. is one of the three certifying bodies accredited by ANAB for the April 15th, 2010 launch of the e-Stewards® program. Orion conducts third party audits to the e-Stewards standard, which “calls for recyclers to eliminate exports of hazardous e-wastes to developing countries; to halt the dumping of such wastes in municipal landfills or incinerators; and to cease the use of captive prison populations to manage toxic e-wastes. It also calls for strict protection of customer’s private data and occupational health safeguards to ensure that workers in recycling plants are not exposed to toxic dusts and fumes” according to the developers of the e-Stewards program.
Read more »
RvA - Certificate
ANAB - Certificate
|