2015 - Webinar On Quality Risk Management for Drugs and Biologics
Date2015-05-29
Deadline2015-05-29
VenueMississauga, Canada
KeywordsHolistic risk management; Risk Control Measures; Drugs and Biologics
Topics/Call fo Papers
Description :
This presentation is intended to help you get familiar with best practices for quality risk management (QRM) applicable to pharmaceutical industry (drugs, biosimilars, and biologics) as well as medical device industry.
This seminar is further intended to discuss how quality risk management can be effectively integrated into a quality system (QS) in the pharmaceutical industry.
This seminar will help attendees understand risk management principles, risk management tools, methods and processes applicable to the pharmaceutical industry. In addition, this seminar will help the attendees how to develop and implement a systematic and holistic risk management strategy integrated into the quality system.
In this 60-min presentation, the speaker will guide you through the details of how to implement the systematic and holistic risk management for drugs, biosimilars, biologics and medical devices.
Areas Covered in the Session :
Laws and Regulations
Key Definitions
Risk Management (RM) Principles
Risk Management Process ? Systematic and Integrated
Risk Management Tools and Methods (PHA, HAZOP, HACCP, FTA, FMEA, FMECA)
Risk Ranking
How to Facilitate Quality Risk Management
Common Mistakes and How to Prevent Common Pitfalls
Risk Control Measures
Risk Communication ? How
RM Applications for Operations, R&D, Materials, Facilities, Utilities, Equipment, Manufacturing, Labeling and Packaging, Laboratory Studies and Quality Control.
Doing RM Right Without Wasting Resources
Practical Aspects (Value) of Risk Management
Interfacing and Relationship with Other Quality Subsystems
Best Practices for Implementing Quality Risk Management in an Efficient and Effective Manner.
Speaker’s Practical PASS-IT Recommendations
Who Will Benefit:
CEOs
VPs
Compliance Officers
Attorneys
Complainant Managers
Managers (RA, QA/QC, CA)
Consultants
Contractors and Subcontractors
Anyone interested in the topic
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
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support-AT-compliancetrainings.com
This presentation is intended to help you get familiar with best practices for quality risk management (QRM) applicable to pharmaceutical industry (drugs, biosimilars, and biologics) as well as medical device industry.
This seminar is further intended to discuss how quality risk management can be effectively integrated into a quality system (QS) in the pharmaceutical industry.
This seminar will help attendees understand risk management principles, risk management tools, methods and processes applicable to the pharmaceutical industry. In addition, this seminar will help the attendees how to develop and implement a systematic and holistic risk management strategy integrated into the quality system.
In this 60-min presentation, the speaker will guide you through the details of how to implement the systematic and holistic risk management for drugs, biosimilars, biologics and medical devices.
Areas Covered in the Session :
Laws and Regulations
Key Definitions
Risk Management (RM) Principles
Risk Management Process ? Systematic and Integrated
Risk Management Tools and Methods (PHA, HAZOP, HACCP, FTA, FMEA, FMECA)
Risk Ranking
How to Facilitate Quality Risk Management
Common Mistakes and How to Prevent Common Pitfalls
Risk Control Measures
Risk Communication ? How
RM Applications for Operations, R&D, Materials, Facilities, Utilities, Equipment, Manufacturing, Labeling and Packaging, Laboratory Studies and Quality Control.
Doing RM Right Without Wasting Resources
Practical Aspects (Value) of Risk Management
Interfacing and Relationship with Other Quality Subsystems
Best Practices for Implementing Quality Risk Management in an Efficient and Effective Manner.
Speaker’s Practical PASS-IT Recommendations
Who Will Benefit:
CEOs
VPs
Compliance Officers
Attorneys
Complainant Managers
Managers (RA, QA/QC, CA)
Consultants
Contractors and Subcontractors
Anyone interested in the topic
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
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support-AT-compliancetrainings.com
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Last modified: 2015-05-11 16:30:27