ComplianceOnline Announces Seminar on SOPs for FDA-Regulated Industry

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ComplianceOnline, the leading GRC advisory network, and regulatory affairs expert, Dr. Mukesh Kumar will conduct a two day seminar on requirements of SOPs for FDA-regulated industries.

ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations. The two day seminar led by renowned regulatory affairs expert Dr. Mukesh Kumar will be held on October 16-17, 2014 in Durham, North Carolina.

This seminar will provide step by step instructions to create SOPs for FDA-regulated organizations based on the instructor’s extensive FDA compliance training experience.

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

Seminar instructor Dr. Mukesh Kumar is a reputed, DC based expert in global regulatory affairs. He leads the regulatory affairs and quality assurance departments at Amarex, a full service pharmaceutical product development company. His areas of expertise also include clinical trials and multi-national project management for medicinal and diagnostic products. He has been a part of over 100 clinical trials in more than 40 countries, presented hundreds of US FDA submissions, conducted numerous training workshops in FDA compliance, and arranged a number of meetings with the FDA.

Throughout the workshop, Dr. Kumar will discuss case studies and examples to highlight regulatory requirements for SOPs, legal requirements for SOP creation and maintenance, and formats and essential components of SOPs. Seminar participants will also comprehend the nuances of compiling effective electronic and paper SOPs.

This course will be beneficial to personnel in all FDA-regulated organizations involved in clinical trials, manufacturing, advertising, marketing, regulatory affairs, auditing, and laboratory testing. Regulatory affair directors, project managers, clinical trial specialists, clinical investigators, quality control personnel, quality assurance managers and auditors will benefit from attending this seminar.

Date: Thursday, October 16 (8.30 AM- 4.30 PM) and Friday, October 17, 2014 (8.30 AM- 4.30 PM)

Location: Durham, North Carolina

Registration Cost: $1,699.00 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

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 ComplianceOnline is a MetricStream portal. MetricStream ( 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
Manager of Program Marketing
2600 E Bayshore Rd
Palo Alto CA USA 94303
650-620-3937 phone
650-963-2530 fax

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ComplianceOnline Announces Seminar on SOPs for FDA-Regulated Industry