Webinar On Good Manufacturing Practices for Medical Devices

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Contact Us 416-915-4458
Webinar On Webinar On Good Manufacturing
Practices for Medical Devices


Presented By Charles Paul
Monday, March 30, 2015 at 1300 Hrs
Hosting By Compliance Trainings
Please visit us at https//compliancetrainings.co
m
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Contact Us 416-915-4458
We Empower, You Comply!
Good Manufacturing Practices for Medical Devices
Product Id
MD1461
Category
Medical Devices
Scheduled On
Monday, March 30, 2015 at 1300 Hrs
Duration
90 Minutes
Speaker
Charles Paul
Login at https//compliancetrainings.com/si
teengine/Login.aspx
Webinar Description
This training concerning Good Manufacturing
Practices is a requirement for all staff involved
in the manufacturer of medical devices.
Regulations are complicated, and today more than
ever before, because of global regulatory
requirements, companies must be familiar with and
comply with the regulations governing the
products they make, for each country in which
they sell. This Webinar will address the
specific requirements of FDA CFR Part 820 and ISO
13485 with some further emphasis upon design
controls and compliance/enforcement.
Areas Covered in the Session
Medical Devices Defined Classifications of
Medical Devices Governing Regulations FDA CFR
Part 820 Review of Subparts A through
O Relationship of FDA CFR Part 820 to ISO
13485 Importance of Design Controls Compliance
and Enforcement Combination Products
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Who Will Benefit

• A must attend webinar for all personnel /
  companies in the Medical Devices industry. The
  professionals who will benefit include all
• Regulatory Affairs
• Quality Professionals
• Product Development Professionals
• Production Department
• QA/QC analysts
• Research Development
• Quality Control
• Quality Assurance scientists
• Quality Auditors
• Internal Auditors
• Operations
• Consultants
• Quality Unit managers and supervisors
• Manufacturing
• Training Managers and Directors
• Documentation department

Price Tags

• Live
• Single Live For One Participant
• 249
• Corporate Live For Max. 10 Participants
• 899
• Recording
• Single REC For One Participant - Unlimited
  Access for 6 Months
• 299

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Speaker Profile
Charles Paul is an instructional designer and
management consultant with over 30 years
experience providing training and consulting
services to regulated industries. He has
installed quality systems and designed and
developed GMP and operational documentation and
training programs for foods and beverage,
pharmaceuticals, biotech, cosmetics, and consumer
product OTC industries.
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tDetailView.aspx?idMD1461
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ings.com support_at_compliancetrainings.com