Browse 84 Life Sciences courses in USA
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Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
Seminar by
ComplianceOnline
This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and ...
Palo Alto
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USD 2,099.00
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This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and ...
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Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
Seminar by
ComplianceOnline
The course is designed for Medical Products Manufacturers. The course will be taught for Medical Devices and Combination Products, but will also be of benefit to Pharmaceutical Manufacturers.
Palo Alto
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USD 2,199.00
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The course is designed for Medical Products Manufacturers. The course will be taught for Medical Devices and Combination Products, but will also be of benefit to Pharmaceutical Manufacturers.
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Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval
Seminar by
ComplianceOnline
The Australian regulatory and reimbursement agency have particular requirements in their assessments of applications for Medical Devices intended for supply in Australia. A well-defined approach or a ...
Palo Alto
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USD 1,499.00
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The Australian regulatory and reimbursement agency have particular requirements in their assessments of applications for Medical Devices intended for supply in Australia. A well-defined approach or a ...
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Exploring Data Integrity To Include FDA, WHO and EMA's Latest Guidance for Industry (2015/2016)
Seminar by
ComplianceOnline
Data Integrity has become a non-compliance area often observed by the FDA and reported within Form FDA 483s and Warning Letters. While various governments have observed this on a world-wide basis, the ...
Palo Alto
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USD 1,899.00
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Data Integrity has become a non-compliance area often observed by the FDA and reported within Form FDA 483s and Warning Letters. While various governments have observed this on a world-wide basis, the ...
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Creating Reader-Focused Technical Documents in FDA Regulated Industries
Seminar by
ComplianceOnline
Advanced technology may have pushed effective communication to the wayside to make clear writing a lost art, now due for revival! In the Information Age, a surplus of technical data proliferates with ...
Palo Alto
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USD 1,699.00
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Advanced technology may have pushed effective communication to the wayside to make clear writing a lost art, now due for revival! In the Information Age, a surplus of technical data proliferates with ...
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FDA's Import Program - New Pathways and Pitfalls
Seminar by
ComplianceOnline
The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier. The FDA and U.S. Customs and Border Protection (CBP) are relying ...
Palo Alto
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USD 1,999.00
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The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier. The FDA and U.S. Customs and Border Protection (CBP) are relying ...
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CGMP Quality Principles for the FDA Regulated Industries
Seminar by
ComplianceOnline
This two-day course is designed for those who work in a Current Good Manufacturing Practices (CGMP) environment and whose roles and responsibilities require they understand and apply quality principles ...
Palo Alto
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USD 1,699.00
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This two-day course is designed for those who work in a Current Good Manufacturing Practices (CGMP) environment and whose roles and responsibilities require they understand and apply quality principles ...
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Data Integrity: FDA/EU Requirements and Implementation
Seminar by
ComplianceOnline
There is no doubt that data integrity is the current and future inspection focus of all regulatory heath care agencies. More than 50% inspection reports such as 483's and Warning Letters quote data integrity ...
Palo Alto
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USD 1,999.00
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There is no doubt that data integrity is the current and future inspection focus of all regulatory heath care agencies. More than 50% inspection reports such as 483's and Warning Letters quote data integrity ...
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FDA Recalls - Before You Start, and After You Finish
Seminar by
ComplianceOnline
FDA's recall authority and program launches you into a project of crisis management. You will learn how to establish a roadmap for conducting recalls. The knowledge you gain will sharpen your recall management ...
Palo Alto
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USD 1,999.00
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FDA's recall authority and program launches you into a project of crisis management. You will learn how to establish a roadmap for conducting recalls. The knowledge you gain will sharpen your recall management ...
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Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
Seminar by
ComplianceOnline
Federal regulation of the advertising and promotion of pharmaceuticals and medical devices reflects an aggressive attitude on the part of the regulators that demands, in turn, that industry be keenly ...
Palo Alto
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USD 1,899.00
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Federal regulation of the advertising and promotion of pharmaceuticals and medical devices reflects an aggressive attitude on the part of the regulators that demands, in turn, that industry be keenly ...
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