ComplianceOnline Announces Seminar on Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

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ComplianceOnline, the leading GRC advisory network, and industry expert, Barry A. Friedman, will conduct a two day seminar on issues and solutions surrounding raw material requirements in a cGMP environment.

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment

ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions. The two day seminar led by industry expert Barry A. Friedman will be held on January 26 and 27, 2017 in Orlando, FL and on March 13 and 14, 2017 in San Francisco, CA.

This interactive seminar will cover issues surrounding raw material requirements in a cGMP environment to ensure compliance with Health Canada, FDA, USP and EP regulations. Dr. Friedman will also host discussions on topics such as compendial vs. non-compendial testing, impact of raw materials in the timely production of a product, use of additional testing and much more. Case studies will be discussed to illustrate regulatory raw material issues.

For more information or to register for the seminar, please click here.

Seminar Instructor Dr. Barry Friedman is a Consultant in the Biotechnology, Regulatory Compliance and Aseptic Processing Arena. Dr. Friedman possesses over 30 years of industrial managerial experience in various aspects of biopharmaceuticals and medical devices to include regulatory compliance, expert witness testimony, GLP/GMP, quality control, auditing, sterility assurance, microbiological/analytical validations and fermentation technology.

This course will be beneficial for quality, regulatory and compliance professionals, manufacturing engineers, quality engineers and auditors. Personnel in research and development, microbiology and documentation will also benefit from this training.

Dates: Thursday, January 26, 2017 (8.30 AM- 4.30 PM) and Friday, January 27, 2017 (8.30 AM- 4.30 PM)
Monday, March 13, 2017 (8.30 AM- 4.30 PM) and Tuesday, March 14, 2017 (8.30 AM- 4.30 PM)
Location 1: Orlando, FL
Location 2: San Francisco, CA
Registration Cost: $1,899.00 per registration
Early bird discounts: For discounts on early registrations, please click here.
Register by phone: Please call our customer service specialists at +1-888-717-2436 or email to customercare(at)complianceonline.com

For more information on ComplianceOnline or to browse through our trainings, please visit our website.

About ComplianceOnline

ComplianceOnline is a leading provider of regulatory compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 35,000 professionals from 9,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at http://www.complianceonline.com. ComplianceOnline is a MetricStream portal. MetricStream (http://www.metricstream.com) is a market leader in Enterprise-wide Governance, Risk, Compliance (GRC) and Quality Management Solutions for global corporations.

For more information please contact:

A Reuben Bernard
Associate Director - ComplianceOnline
2600 E Bayshore Rd
Palo Alto CA USA 94303
Phone - +1-650-238-9656 | +1-888-717-2436
Fax - 650-963-2556
Mail: reuben(at)complianceonline.com
Website: http://www.complianceonline.com

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A Reuben Bernard
@Compliance_On
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