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FDA Regulatory Seminars for Life Science Industry Professionals
ComplianceOnline, a leading GRC Advisory Network, will conduct a comprehensive series of seminars focused on regulatory issues affecting the life sciences industry in January 2012.
PALO ALTO, Calif., Dec. 14, 2011 /PRNewswire/ -- ComplianceOnline, a leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced an exciting roster of in-person seminars for the life sciences industry in January 2012.
A large number of life science professionals are expected to attend these seminars which will be held in various cities, including San Francisco, San Diego and Salt Lake City. Please visit our site for more information or to register for FDA Regulatory seminars.
The seminars will be led by some of the most experienced and respected experts in the life sciences industry.
The first ComplianceOnline seminar for 2012 is Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina), led by Robert J Russell, the highly respected authority on global regulatory issues.
This two-day long seminar will be held in San Francisco, CA on January 19 and 20, 2012. It covers topics ranging from pre-clinical/ clinical requirements, product registration, amendments and renewals for life science products in Latin America, with a strategic focus on how to work with regulatory agencies in Latin America.
The next seminar, Understanding and Implementing the Medical Device Directive, will be held on January 26 and 27 in San Diego, CA. Dan O'Leary, a quality and operations expert with more than 30 years of experience will help seminar attendees comprehensively understand details of the MDD and implement its requirements. During the course, participants will have exercises that apply the principles and help solidify learning.
On January 27, 2012, a seminar entitled Clear as Mud: Obtaining & Marketing your 510(K) with Today's FDA will be held in Salt Lake City, Utah. Jointly led by Mark DuVal and Mark Gardner - nationally renowned attorneys and experts on FDA regulations - this full day seminar will teach medical device industry professionals strategies to ensure that they obtain 510(k) from the FDA in a cost-effective and efficient manner.
The last seminar for January - Statistical Considerations for ICH Guidelines - is scheduled for Jan 30 and 31 in San Francisco. This unique hands-on course, led by Steven Walfish, will provide attendees with an understanding of how to apply to Statistics to the ten ICH Quality guidelines. The course will deliver tools, templates and insight that will allow participants to immediately begin implementation within their organization/firm.
For early bird discounts, please Click here.
Please visit here for more information on ComplianceOnline
About ComplianceOnline
ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 15,000 professionals from 3,000 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.
Media contact:
Email: priya@complianceonline.com
Phone: 650-620-2955
SOURCE ComplianceOnline
ComplianceOnline
Web Site: http://www.complianceonline.com
FDA Regulatory Seminars for Life Science Industry Professionals
ComplianceOnline, a leading GRC Advisory Network, will conduct a comprehensive series of seminars focused on regulatory issues affecting the life sciences industry in January 2012.
PALO ALTO, Calif., Dec. 14, 2011 /PRNewswire/ -- ComplianceOnline, a leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced an exciting roster of in-person seminars for the life sciences industry in January 2012.
A large number of life science professionals are expected to attend these seminars which will be held in various cities, including San Francisco, San Diego and Salt Lake City. Please visit our site for more information or to register for FDA Regulatory seminars.
The seminars will be led by some of the most experienced and respected experts in the life sciences industry.
The first ComplianceOnline seminar for 2012 is Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina), led by Robert J Russell, the highly respected authority on global regulatory issues.
This two-day long seminar will be held in San Francisco, CA on January 19 and 20, 2012. It covers topics ranging from pre-clinical/ clinical requirements, product registration, amendments and renewals for life science products in Latin America, with a strategic focus on how to work with regulatory agencies in Latin America.
The next seminar, Understanding and Implementing the Medical Device Directive, will be held on January 26 and 27 in San Diego, CA. Dan O'Leary, a quality and operations expert with more than 30 years of experience will help seminar attendees comprehensively understand details of the MDD and implement its requirements. During the course, participants will have exercises that apply the principles and help solidify learning.
On January 27, 2012, a seminar entitled Clear as Mud: Obtaining & Marketing your 510(K) with Today's FDA will be held in Salt Lake City, Utah. Jointly led by Mark DuVal and Mark Gardner - nationally renowned attorneys and experts on FDA regulations - this full day seminar will teach medical device industry professionals strategies to ensure that they obtain 510(k) from the FDA in a cost-effective and efficient manner.
The last seminar for January - Statistical Considerations for ICH Guidelines - is scheduled for Jan 30 and 31 in San Francisco. This unique hands-on course, led by Steven Walfish, will provide attendees with an understanding of how to apply to Statistics to the ten ICH Quality guidelines. The course will deliver tools, templates and insight that will allow participants to immediately begin implementation within their organization/firm.
For early bird discounts, please Click here.
Please visit here for more information on ComplianceOnline
About ComplianceOnline
ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 15,000 professionals from 3,000 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.
Media contact:
Email: priya@complianceonline.com
Phone: 650-620-2955
SOURCE ComplianceOnline
ComplianceOnline
Web Site: http://www.complianceonline.com