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The American Society for Quality (ASQ)

The following information was provided courtesy of ASQ, and is not meant as an endorsement of CfPA products. It serves only as an informational guide about the certifications offered by ASQ.

The American Society for Quality (ASQ) is the world's leading authority on quality. With more than 95,000 individual and organizational members, this professional association advances learning, quality improvement, and knowledge exchange to improve business results, and to create better workplaces and communities worldwide.

As champion of the quality movement, ASQ offers technologies, concepts, tools, and training to quality professionals, quality practitioners, and everyday consumers, encouraging all to Make Good Great®.

Since 1991 ASQ has administered the United States’ premier quality honor— the Malcolm Baldrige National Quality Award, which annually recognizes companies and organizations that have achieved performance excellence.

ASQ offers 14 certification programs: Certified Quality Engineer, Certified Quality Auditor, Certified Manager of Quality Organizational Excellence, Certified Software Quality Engineer, Certified Reliability Engineer, Certified Quality Technician, Certified Quality Inspector, Six Sigma Black Belt, Six Sigma Green Belt, Certified HACCP Auditor, Certified Biomedical Auditor, Certified Calibration Technician, Certified Quality Improvement Associate, Certified Quality Process Analyst.

For more information about ASQ, contact them at:


    American Society for Quality
    600 North Plankinton Avenue
    Milwaukee, WI 53203 USA
    North America: 800-248-1946
    Fax: 414-272-1734
    E-mail: help@asq.org
    Website: www.asq.org


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Courses With
This Accreditation

Analytical Methods Validation for FDA Compliance
Sep 13 2010
, Burlingame, CA

CMC Submissions in CTD Format
Sep 20 2010
, Burlingame, CA

Documentation Management and Control
Sep 27 2010
, East Brunswick, NJ

Preparation, Packaging and Labeling of Clinical Trial Materials
Sep 27 2010
, East Brunswick, NJ

Preparing for and Surviving an FDA Inspection
Sep 29 2010
, East Brunswick, NJ

Lyophilization Technology
Oct 12 2010
, New Brunswick, NJ

Design Control and Product Validation
Oct 18 2010
, New Brunswick, NJ

Preparation, Packaging and Labeling of Clinical Trial Materials
Oct 18 2010
, Amsterdam, The Netherlands

Developing and Maintaining an Effective Complaint System
Oct 20 2010
, New Brunswick, NJ

Analytical Methods Validation for FDA Compliance
Oct 25 2010
, Amsterdam, The Netherlands

Conducting Effective Quality Audits
Oct 25 2010
, New Brunswick, NJ

Root Cause Investigation for CAPA
Nov 02 2010
, New Brunswick, NJ

CMC Submissions in CTD Format
Nov 04 2010
, Amsterdam, The Netherlands

Microbiological Control and Validation
Nov 08 2010
, Amsterdam, The Netherlands

Critical Process Cleaning and Cleaning Validation
Dec 01 2010
, Amsterdam, The Netherlands

Drug Product Stability and Shelf-Life
Dec 13 2010
, Amsterdam, The Netherlands

ICH-Q7
Dec 13 2010
, Amsterdam, The Netherlands

Active Pharmaceutical Ingredients
840

Active Pharmaceutical Ingredients
840

Aerosol Technology
669

Annual Product Reviews (APRs) For Pharmaceuticals
1998

Annual Product Reviews (APRs) For Pharmaceuticals
1998

Applied cGMPs for Pharmaceutical and Allied Industries
610

Atomization, Sprays and Atomizers
1883

Calibration in the FDA Regulated Industry
2026

cGTP in a Nutshell
2179

cGTP in a Nutshell
2179

Combination Product Development: Safety/Registration/Approval
2104

Current Good Manufacturing Practice (cGMP) for Purchasing
1836

Current Good Tissue Practices (cGTPs)
2086

Early Stage Clinical Studies for Drugs and Devices
2118

Elements of Applied Process Engineering
1512

Suspensions and Emulsions in Pharmaceuticals and Food
274

Excipient GMPs
2050

Food Extrusion Technology
689

Fundamentals of Nanotechnology
2111

GMP for Dietary Supplements
2094

Good Distribution Practices
2116

Good Laboratory Practices (GLP)
545

Granulation, Tabletting and Capsule Technology
541

ICH Q10: Pharmaceutical Quality System
2131

Safety Assessment of Cosmetic Ingredients and Formulations
2161

INDs/NDAs/CTDs
448

INDs/NDAs/CTDs
448

Industrial Ink Technology
1579

IQ, OQ, PQ
1808

ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
2092

Laboratory Control System
2047

Laboratory Control System
2047

Machinery Failure Analysis and Prevention (US Course)
1054

Medical Device Regulatory Compliance
1992

Microbiological Quality of Water-Based Consumer Products
1383

Non-Clinical Drug Safety Evaluation and Drug Development
1153

Packaging of Pharmaceuticals
42

PAT Online Process Analysis
2030

Applied cGMPs for Pharmaceutical and Allied Industries
610

Pharmaceutical Process Development
1358

Pharmaceutical Quality Assurance and Control
224

Pharmaceutical Technology Transfer
2095

Pilot Plant and Scale-up Studies
1882

Real World Approaches to PAT and QbD Implementation
2085

Real World Approaches to PAT and QbD Implementation
2085

Real World Approaches to PAT and QbD Implementation
2085

Process Validation for the Pharmaceutical and Medical Device Industries
736

REACH: Registration, Evaluation and Authorization of Chemicals
2145

Regulatory Compliance for the Personal Care Products Industry
1522

Risk Management Today: Complying with the ISO 14971: 2007 Standard
2106

Risk Management Today: Complying with the ISO 14971: 2007 Standard
2106

Role of PAT and QbD in Biologic Drug Production
2163

Sterile Products: Formulation, Manufacture and Quality Assurance
435

Sterilization in the Pharmaceutical Industry
2075

Suspensions and Emulsions in Pharmaceuticals and Food
274

System Validation, GAMP Harmonization and P.A.T
913

System Validation, GAMP Harmonization and P.A.T
2203

Tablet Production for Operators and Supervisors
1428

Vendor and Contract Supplier Qualification
1984

Writing and Implementing Clinical Protocols
772

Writing SOPs for cGMP Compliance
1646