Expert Profile
Robert J Russell
President and CEO, RJR Consulting, Inc
Bob is a Global Regulatory and CMC expert with 28 years of prior industry experience in international regulatory management and compliance, global business development and global supply chain management. Mr. Russell formerly held senior leadership positions, in these functional areas, at Dow Pharmaceuticals and Cordis-Dow Medical Devices.
His experience and knowledge span Healthcare Authority’s requirements and regulatory processes across Life Science products.
For the past 18 years, Bob has been President & CEO of RJR Consulting, Inc. The company assists the pharmaceutical, medical device and biotech industries in understanding Regulations affecting compliance and in conducting product registrations with their clients in more than 95 countries.
He holds a BS / MS in Chemistry.
Trainings by Expert
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences PART I
Category:
Medical Devices
,
Biotechnology
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
The EU Clinical Trial Directive
Category:
Medical Devices
,
Life Sciences
Latin America - Understanding Regulatory Compliance Requirements Across Life Science Industry PART I
Category:
Drugs and Chemicals (Pharma)
,
Medical Devices
,
Biotechnology
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
European Filing and Registration Procedures
Category:
Drugs and Chemicals (Pharma)
,
Medical Devices
,
Biotechnology
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences PART II
Category:
Medical Devices
,
Clinical Research
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
Latin America - Understanding Regulatory Compliance Requirements Across Life Science Industry Part II
Category:
Drugs and Chemicals (Pharma)
,
Medical Devices
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences PART I & PART II
Category:
Drugs and Chemicals (Pharma)
Webinar - Latin America – Understanding Regulatory Compliance Requirements Across Life Science Industry PART I & PART II
Category:
Medical Devices
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities
Category:
Drugs and Chemicals (Pharma)
,
General Manufacturing
,
Biotechnology
,
Quality and Safety
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Life Sciences
,
Documentation and Data Management
Updated EU filing and registration procedures (including the new variation rules coming in to force)
Category:
Drugs and Chemicals (Pharma)
,
Medical Devices
,
Biotechnology
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
