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.

1. Webinar On Webinar On Good
Manufacturing Practices for Medical Devices
Presented By Charles Paul
Contact Us: 416-915-4458
Hosting By
Compliance Trainings
Please visit us at https://compliancetrainings.com
Monday, March 30, 2015 at 13:00 Hrs

2. Contact Us: 416-915-4458
We Empower, You Comply!
Webinar Description:
Good Manufacturing Practices for Medical Devices
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.
Product Id MD1461
Category Medical Devices
Scheduled On Monday, March 30, 2015 at 13:00 Hrs
Duration 90 Minutes
Speaker Charles Paul
Login at https://compliancetrainings.com/siteengine/Login.aspx
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

3. 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

4. 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.
To Register This Webinar Please Visit
https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1461
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