Apply For Accreditation

All Applicants shall fill Part I & Part III while Part II will be filled according to each of their specific scheme eg. ISO/IEC 17025, 17020, 17065, 17043, 17024... etc.
					

Part I : General Information

LOGIN CREDENTIAL

INSTRUCTIONS:

1. Your application cannot be processed unless attached with the required document in soft(pdf/docs/jpg/png) copies.
									2.	Additional advice or information may be obtained by contacting the relevant PAC accreditation manager as displayed on PAC website or by emailing us on info@pacofusa.org.
									3.	Granting accreditation will be subject to the applicant entity fully complying with the accreditation criteria, PAC accreditation requirements and PAC regulation.
									4.	The applicant is specifically advised to read relevant PAC information pack before applying for accreditation.
									5.	If the applicant does not receive an Acknowledgement of receipt of this form, please contact PAC relevant accreditation manager by emailing us on info@pacofusa.org.
									

A) INFORMATION ABOUT CAB

B) PLEASE COMPLETE THE BELOW INFORMATION REGARDING CAB

CAB Key Location: Entities performing and/or managing key management system certification activities, on behalf of accredited certification bodies, which are wholly or partly owned or employed by the CAB.
Subcontractor Key Location: Entities performing and/or managing key management system certification activities, on behalf of accredited certification bodies, which are not wholly or partly owned or employed by the CAB.
Subcontractor: Entities performing and/or managing processes related to management system activities, on behalf of accredited certification bodies, which are not wholly or partly owned or employed by the CAB (processes include; marketing, communications, outreach, etc. This list is not all-inclusive; any non-key activity related to the accredited CB's certification program is applicable.)

C) Information About Ownership (Legal status of your organization)
Please tick the appropriate box.

D) OTHER DESCRIPTION OF THE THE ORGANIZATION SEEKING ACCREDITATION

Name and position (Director level) of person authorizing this application

Technical/Scheme Manager

Quality Manager

E) INDICATE EXACTLY HOW THE NAME OF YOUR CAB APPEARS ON THE ACCREDITATION CERTIFICATE

F) INTERNAL AUDIT AND MANAGEMENT REVIEW

G) LOCAL REGULATION
Please mention the current regulation / law that related to your organization activities.

Name of the Regulation/Law Issue Date Item(s) related to the applied scope

H) OTHER ACCREDITATION/CERTIFICATIONS (INCLUDING PAC ACCREDITATION)

Are you currently accredited or have you been accredited within the past five years.
If YES, please provide the name of Accreditation body and the current expiration date of accreditation. If no longer accredited, provide the approximate end date of accreditation.
Please note below if your accreditation has ever been Suspended/Cancelled
Please provide the approximate date of Suspension/Cancellation
Reason For Suspension/Cancellation
Was your Accreditation fully reinstated after the Suspension/Cancellation

I) APPLICANT OUTSIDE USA
Applicants from outside country will be processed according to ILAC-G21(Cross-Frontier Accreditation Principles for Cooperation), IAF MD12 (Accreditation Assessment of Conformity Assessment Bodies with Activities in Multiple Countries)

Is there a local accreditation body?
Is the local accreditation body a signatory to the arrangement of ILAC, IAF?
Does the local accreditation body offer the required scope?
Do you permit:
That PAC informs the local accreditation body about your application and the development of the accreditation process?
That the local accreditation body may send an observer to join the assessment?
That the local accreditation body may send (an) assessor/s (joint assessment for a dual accreditation)?

J) NAME(S) OF COUNTRIES WHERE CAB INTENDS TO PROVIDE PAC ACCREDITED CERTIFICATIONS

K) RELATIONSHIP AND SISTER CONCERN RELATED INFORMATION

Other activities of CAB
Details
Relationship in a larger entity if any, addresses of all its physical location(s) and, information on activities conducted at all locations including virtual site(s)
Related Bodies of CAB's top management (Please include complete details of all BODs & share holders)
Activities executed by the related bodies
Requirement for preliminary visit prior to the commencement of assessment process

Part II: Inforamtion About Scheme Seeking Accreditation

SELECT THE SCHEME SEEKING ACCREDITATION

Section II.I : Testing Laboratory (TL) - ISO/IEC 17025

A. FIELD FOR WHICH ACCREDITATION IS SOUGHT: (Please tick the appropriate boxes)

B. SCOPE OF TESTING FOR WHICH ACCREDITATION IS SOUGHT:

Materials/Product Tested
Types of Test/Properties Measured
Range of Measurement
Standard/Specifications/Techniques used

C. LIST THE MAJOR ITEMS OF EQUIPMENT CURRENTLY USED FOR THE TYPES OF TEST:

Description of equipment
(Include Manufacturer, Model& Serial number/Code number)
Range/ Capacity of equipment and other relevant information

D. PLEASE INDICATE THE TYPE OF CALIBRATION FOR THE TESTING LAB EQUIPMENT:

* In case of internal calibration for equipment used, please fill in the following details for the scope of the internal calibration.

Please indicate the type of calibration sites:
 
Measured Quantity
Range
Calibration & Measurement
Capability (#) Uncertainity
Brief Description of Measurement
and Equipment Used

Section II.II : Calibration Laborator (CL) - ISO/IEC 17025

A) FIELD FOR WHICH ACCREDITATION IS SOUGHT: (Please tick the appropriate boxes)

B) SCOPE OF CALIBRATION FOR WHICH ACCREDITATION IS SOUGHT:

Measured Quantity
Range
Calibration & Measurement (Capability)*

C) LIST THE MAJOR ITEMS OF EQUIPMENT CURRENTLY USED FOR THE TYPES OF CALIBRATION:

Description of equipment
(Include Manufacturer, Model & Serial/Code number)
Range/Capacity of equipment
and other relevant information

D) PLEASE INDICATE THE TYPE OF CALIBRATION LAB EQUIPMENT:

* In case of internal calibration for equipment used, please fill in the following details for the scope of the internal calibration.

Please indicate the type of calibration sites:
 
Measured Quantity Range Calibration & Measurement
Capability (#) Uncertainity
Brief Description of Measurement
and Equipment Used

Section II.III : Medical Laboratory (ML) - ISO 15189

A) FIELD FOR WHICH ACCREDITATION IS SOUGHT: (Please tick the appropriate boxes)

B) DETAILS OF PRIMARY SAMPLE COLLECTION FACILITIES:
(Please mention clearly with full addresses the primary sample collection facilities)

Primary sample collection facility
Address

C) LABORATORY BRANCHES: DOES THE LABORATORY HAVE BRANCHES?

PLEASE MENTION CLEARLY WITH FULL ADDRESSES THE LABORATORY BRANCHES WITHIN THE ACCREDITATION SCOPE:

Branch
Address

DO THE LABORATORY BRANCHES HAVE SEPARATE MANAGEMENT SYSTEMS?

LIST OF MEDICAL SCOPES AND MAJOR ITEMS OF EQUIPMENT CURRENTLY USED:

Discipline/Types of Tests (Department) Standard Specifications / Techniques Used / Equipment
Name of test Method name and Reference Equipment name and SN

D) PLEASE INDICATE THE TYPE OF MEDICAL LAB EQUIPMENT:

* In case of internal calibration for equipment used, please fill in the following details for the scope of the internal calibration.

Please indicate the type of calibration sites:
 
Measured Quantity
Range
Calibration & Measurement
Capability (#) Uncertainity
Brief Description of Measurement
and Equipment Used

Section 2.4: Inspection Body (IB) - ISO/IEC 17020

A. FIELD FOR WHICH ACCREDITATION IS SOUGHT: (Please tick the appropriate boxes)

 

B. SCOPE OF INSPECTION FOR WHICH ACCREDITATION IS SOUGHT:

Field of Inspection
such as :product design, products (specified as materials or equipment) Installations, plant, premises, processes, services and surveys
Type and Range of Inspection
e.g. In-service inspection or inspection of new products
Methods and Procedures
such as:EC directives, regulations, standards, specifications, internal procedures

C. FOR WHOM DOES THE INSPECTION BODY UNDERTAKE INSPECTION?

D. WHAT DO YOU CONSIDER TO BE THE TYPE OF YOUR INSPECTION BODY, AS DEFINED IN ISO/IEC 17020

E. DO YOU PERFORM INSPECTION OUTSIDE USA ?

If yes state the countries in which inspections performed

F. PLEASE INDICATE THE TYPE OF CALIBRATION FOR THE INSPECTION BODY EQUIPMENT:

* In case of internal calibration for equipment used, please fill in the following two tables for the scope of the internal calibration:

Please indicate the type of calibration sites:

 
Measured Quantity
Range
Calibration & Measurement
Capability (#) Uncertainity
Brief Description of Measurement
and Equipment Used

Section 2.5: MS Certification Body (MsCB) - ISO/IEC 17021-1

IDENTIFY THE MANAGEMENT SYSTEM CERTIFICATION SCHEME(S) FOR WHICH ACCREDITATION IS SOUGHT:

CERTIFICATION AREA
SCOPE
Countries
QMS-ISO 9001
supplementary accreditation standard for this certification area is ISO/IEC 17021-3
IAF Codes according to IAF MD 17  
EMS-ISO 14001
supplementary accreditation standard for this certification area is ISO/IEC 17021-2
OH SMS-ISO 45001
supplementary accreditation standard for this certification area is ISO/IEC TS 17021-10:2018 & IAF MD 22:2018
FSMS-ISO 22000
supplementary accreditation standard for this certification area is ISO/TS 22003
FSMS subcatagory according to Table A.1 - Food chain categories of ISO/TS 22003 :2013  
ISO 37000
Supplementary accreditation standard for this certification area is ISO/TEC TS 17021-9:2016
Subcatagory According to ISO/TEC TS 17021-9:2016 Normative documents Countries
EnMS-ISO 50001
supplementary accreditation standard for this certification area is ISO 50003
EnMS Technical areas according to ISO 50003
Technical Area
Description of technical areas for EnMS
Countries
MDQMS-ISO 13485
Supplementary accreditation standard for this certification area is IAF MD 9
Scope According to IAF MD 9
Main Technical Areas
Product Categories Covered by the Technical Areas
Countries
ISMS-ISO 27001
Supplementary accreditation standard for this certification area is ISO/IEC 27006
MS ISO 21001
Educational organizations
Supply chain security Management Systems - according to ISO 28001. Supplementary accreditation standard for this certification area is ISO 28003
Other
(Please mention details)

Section 2.6: Proficiency Testing Provider (PTP) - ISO/IEC 17043

Activity/Services
Select appropriate proficiency testing items
Done by
Collaborator/Sub-contractor Location / Contact details
Accreditation / Certification held including PAC accreditation
PTP
Collaborator
Subcontractor
Plan the PT scheme
Perform sampling
Conduct measurements to determine stability and homogeneity
Determine assigned values and associated uncertainties of the measurands
Prepare, handle, packaging, labeling and distribution of proficiency test items
Provide instructions for participants
Operate the data processing system
Develop statistical design
Conduct statistical analysis
Evaluate the performance of proficiency testing scheme participants
Give opinions and interpretations
Authorize the issue of proficiency testing report

COLLABORATORS / SUBCONTRACTORS INFORMATION:

Please complete this table for all collaborator/subcontractors with which the proficiency testing provider has formal arrangements for the production, testing, measurement, sampling, storage, and distribution of the PT materials/samples or measurement artifacts, and for data processing.
Subcontractor / Collaborator Name and address
Accreditation held(if applicable)
Activities/services rendered

Scope of proficency testing for which accreditation is sought:

Sample/ Artifact Sample
Tests/ Properties measured
Scheme Title/ Type
Frequency

Section 2.7: Product Certification Body (PdCB) - ISO/IEC 17065

CONFORMITY EVALUATION IN THE FIELD (Product, Process and/or Service Groups):

THE CERTIFICATION SCHEMES, STANDARDS OR NORMATIVE DOCUMENTS::

SCOPE OF PRODUCT, PROCESS AND/OR SERVICE GROUPS FOR WHICH ACCREDITATION IS SOUGHT(Conformity Assessment Procedures to be Accredited):

Product (s) / Product Group (s)
Certification Standard / Scheme

GENERAL INFORMATION:

Is the certification body already accredited or applied for accreditation by another accreditation body?
If the answer is yes fill the following:
Accreditation body name Date of application
Fields of conformity evaluation which are accredited or for which accreditation has been applied:
Approvals and other recognitions of the certification body:
DOCUMENTED STRUCTURE TO SAFEGUARD IMPARTIALITY
WHO ARE THE STAKEHOLDERS REPRESENTED IN THIS STRUCTURE (COMMITTEE)?

STAFF OF THE CERTIFICATION BODY

Number of
Staff
Other staff (Part-time workers)
Persons with university education
Persons with technical school education
Persons trained in quality management

CERTIFICATION PROCEDURES

What are the rules and procedures of certification for the fields of conformity listed in the application?
Are the proposed certification systems for accreditation described by own procedure and administration rules?
Does the certification body have special departments, groups or technical committees responsible for determined fields of certification?
If YES, Information on the special field (name, address):
Does the certification body itself carry out tests of products, processes and services in the fields of certification applied for?
Is there an accreditation of the testing laboratories of the certification body?
If YES, By which accreditation bodies?:
Fields of testing:
Does the certification body itself carry out the surveillance of products, processes and services in the fields of certification applied for?
Who are the subcontractors for surveillance visits?
Which testing laboratories work for the certification body?
Name / Identification
Test fields
Accredited by
In the case of non-accredited subcontractors, in which way does the certification body make sure that it complies with the requirements of the concerning international documents (e.g. ISO/IEC 17025)?

QUALITY SYSTEM

Does the certification body have a quality manual?
Has a quality manager been appointed
If YES, Name
To ensure the compliance with the criteria of the standard ISO/IEC 17065, are there Internal audits and repetitive checks?
Where are they documented?
Which arrangements are made to ensure confidentiality?
Is there a procedure for handling of complaints against decisions of the certification body?

Section 2.8: Person Certification Body (PsCB) - ISO/IEC 17024

A. Does the applying organization/ certification body operate additional locations / test centres:
Locations of the applicant organization/ certification body:
Address
PO Box / Code
City
*Org. chart Please attach the organisational structure (the structure within an organisation) of the certification body.
B. Identify the certification scheme for persons for which accreditation is sought:

C. GENERAL INFORMATION

Is the certification body already accredited or applied for accreditation by another accreditation body?
If the answer is yes fill the following:
Accreditation body name Date of application
Fields of conformity evaluation which are accredited or for which accreditation has been applied:
Approvals and other recognitions of the certification body:
D. DOCUMENTED STRUCTURE TO SAFEGUARD IMPARTIALITY
E. WHO ARE THE STAKEHOLDERS REPRESENTED IN THIS STRUCTURE (COMMITTEE)?

F. STAFF OF THE CERTIFICATION BODY

Number of
Staff
Other staff (Part-time workers)
Persons with university education
Persons with technical school education
Persons trained in quality management

G. Certification Scheme

Accepted personal certification scheme including quality procedures for verification and certification, quality manual:
Owner / authors of the personal certification scheme (if different form applicant organization/ certification body):
Interested parties represented in the scheme (scheme committee):
Is the scheme nationally / internationally accepted within the industry?

H. Quality system

Do the applicant organization / the certification body complywith any standard for quality system?
If YES, which one?
Has a quality manager been appointed
If YES, Name
Is there a documented system for internal quality audits to ensurethe compliance with ISO 17024?
Are there documented procedures to ensure confidentiality?
Are there procedures regarding the misuse of certificates?
Is a description of the certification system available in published form?

I. Scope of Application

Certification Scheme for Persons
Sector
Method & Level

Part III : Declaration by the Applicant

Declaration:

  • I declare that I am authorized, on behalf of the organization to submit this application, and that the information contained herein is both correct and accurate to the best of my knowledge and belief.
  • Upon accreditation the organization agrees to comply with PAC requirements.
  • I will enclose a copy of the quality manual (if any), PAC relevant Assessment Checklist Report, relevant procedures, the application fees and any needed documentation(s).
  • I understand the manner by which the accreditation system operates and functions.
  • I agree to cooperate with the visit assessment team appointed by PAC for examination of all relevant documents by them and their visits to those parts of the CAB which are part of the scope of the accreditation.
  • I agree to comply with the accreditation procedures, pay all the costs for pre-assessment (if any), initial assessment, sequential assessment and re-assessment.
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