Quality Agreements Made Easy (Advanced 2018)
Training
Online
*Indicative price
Original amount in USD:
$ 150
Description
-
Type
Training
-
Level
Advanced
-
Methodology
Online
-
Class hours
1h
-
Duration
1 Day
-
Start date
Different dates available
-
Virtual classes
Yes
The specification developer must be aware of the capabilities of the contract manufacturer and the contract manufacturer must be aware of the limitations of the specification developer, for example.
Facilities
Location
Start date
Start date
Reviews
Subjects
- Compliance Trainings
- Quality Assurance
- Online Trainings
- Courses
- Medical training
- Professional
- Manufacturing
- Pharmaceutical
- Medical Trials
- Healthcare
Teachers and trainers (1)
Adam Fleming
Event Manager
Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements.
Course programme
Why should you Attend:To the extent that anyone responsible within a specification developer, contract design organization, purchasing organization, supplier of critical or crucial materials or services, or contract manufacturing and/or testing organization is concerned about conformity to the ISO 13485:2016 or compliance to the FDA regulations and imminent European Medical Device Regulation, this webinar is for you.
Areas Covered in the Session:What are the consequences of mistakes in quality agreements?How hard does drafting a meaningful quality agreement have to be?What do regulators look for in these quality agreements?How often should a quality agreement be reviewed? Revised?What if I cannot achieve agreement with the other party?Tips for making a quality agreement acceptable to all
Who Will Benefit:Regulatory ManagementRegulatory ConsultantsQuality ManagementSales & Marketing ManagementScientific Staff (Advisors)Clinical Staff (Advisors)Research & Development Management
Speaker Profile:Shep Bentley is the President and Principal Consultant for Bentley Biomedical Consulting, LLC, where he is responsible for regulatory strategies leading to FDA approvals and clearances for digital medical device companies. Shep began his career in 1984 at the Hospital Corporation of America as a research technician, and worked at McGaw Labs in Irvine, responsible for GMPs until 1989, when he joined TOSHIBA America where he managed production of various digital devices.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: support@compliance4All.com
Additional information
Quality Agreements Made Easy (Advanced 2018)
*Indicative price
Original amount in USD:
$ 150