Browse 87 courses in USA
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Courses > Health, Safety & Security > Medical Laboratory / Technology
Medical Laboratory / Technology
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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Phlebotomy Certification Class - Oregon
Training by
Phlebotomy Training Specialists
We offer Daytime, Evening and Weekend programs to fit any schedule. Classes typically start the around the beginning of each month. The National Phlebotomy Classes that we offer in several different states ...
Utah
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We offer Daytime, Evening and Weekend programs to fit any schedule. Classes typically start the around the beginning of each month. The National Phlebotomy Classes that we offer in several different states ...
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7402 - Steam Production
Online Free Online Course by
360training.com
The objective of this second module is to look at the concept of steam generation, and to present features of design and construction of boilers (steam generators). Both the water side and gas side ...
Online Live
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FREE Online Free Online Course
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The objective of this second module is to look at the concept of steam generation, and to present features of design and construction of boilers (steam generators). Both the water side and gas side ...
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PCT=C.N.A. + EKG + Phlebotomy
Training by
Access Institute
Description: This course is intended to provide the understanding of basic principles of blood drawing, practicing blood draw on artificial arm, identification of color coded tubes, common sites of venipuncture ...
Kew Gardens
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Description: This course is intended to provide the understanding of basic principles of blood drawing, practicing blood draw on artificial arm, identification of color coded tubes, common sites of venipuncture ...
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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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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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Quality Control Laboratory Compliance - cGMPs and GLPs
Seminar by
ComplianceOnline
FDA inspection and oversight of quality control (QC) laboratories are essential elements of the agency’s evaluation of the compliance status of regulated companies representing multiple industries - pharmaceuticals, ...
Palo Alto
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USD 2,099.00
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FDA inspection and oversight of quality control (QC) laboratories are essential elements of the agency’s evaluation of the compliance status of regulated companies representing multiple industries - pharmaceuticals, ...
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Supplier Management for Medical Device Manufacturers
Seminar by
ComplianceOnline
Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide components to the device manufacturer, which means that they are critical to performance ...
Palo Alto
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USD 1,999.00
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Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide components to the device manufacturer, which means that they are critical to performance ...
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Meeting ILAC Requirements for Measurement Traceability to the SI through NIST and other National Metrology Institutes
Seminar by
ComplianceOnline
More regulatory agencies are now specifying requirements for test and calibration results to be supported by Traceability of Measurement that conforms to ILAC P10. Regulators now believe that Traceability ...
Palo Alto
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USD 1,899.00
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More regulatory agencies are now specifying requirements for test and calibration results to be supported by Traceability of Measurement that conforms to ILAC P10. Regulators now believe that Traceability ...
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Phlebotomy Technician Training
Training by
Ace Computer Training Center
This course teaches students to: Define phlebotomy and understand the role of phlebotomist Identify types and structures of blood vessels Describe guidelines for patient relations Describe safety procedures ...
Queens
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This course teaches students to: Define phlebotomy and understand the role of phlebotomist Identify types and structures of blood vessels Describe guidelines for patient relations Describe safety procedures ...
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21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
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Online Webinar by
Training Doyens
OVERVIEW The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part ...
Online
USD 159.00
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OVERVIEW The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part ...
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GMPs Applied to Medical Cannabis: All You Need to Know
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Online Webinar by
Training Doyens
OVERVIEW When we discuss growing, producing, and manufacturing medical cannabis, we must think of it as a medicine. Medicine by definition, it is a substance intended to assist you with a medical condition, ...
Online
USD 159.00
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OVERVIEW When we discuss growing, producing, and manufacturing medical cannabis, we must think of it as a medicine. Medicine by definition, it is a substance intended to assist you with a medical condition, ...
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FDA's Guidance on Software and Device Changes and the 510(k)
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Online Webinar by
Training Doyens
OVERVIEW The FDA has provided two guidance documents on software and device changes, which provide information as to whether a new 510(k) is needed. The first guidance document clarifies key terms and ...
Online
USD 159.00
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OVERVIEW The FDA has provided two guidance documents on software and device changes, which provide information as to whether a new 510(k) is needed. The first guidance document clarifies key terms and ...
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Data Integrity for the Laboratory and Beyond - Careful Considerations for Your Next Audit
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Online Webinar by
Training Doyens
OVERVIEW Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition ...
Online
USD 159.00
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OVERVIEW Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition ...
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Data Integrity for the Laboratory and Beyond - Careful Considerations for Your Next Audit
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Online Webinar by
Training Doyens
OVERVIEW Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition ...
Online
USD 199.00
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OVERVIEW Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition ...
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Developing a Strategic Approach to FDA Compliance for Computer Systems
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Online Webinar by
Training Doyens
OVERVIEW FDA requires that all computer systems used to produce, manage and report on GxP (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. You’ll learn all ...
Online
USD 159.00
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OVERVIEW FDA requires that all computer systems used to produce, manage and report on GxP (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. You’ll learn all ...
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Medical & Recreational Marijuana: Impact on the 2020 Workplace
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Online Webinar by
Training Doyens
OVERVIEW There are currently more questions than answers on the subject of the legalization of medical and recreational marijuana and how does medical marijuana affect the workplace. The debate of the ...
Online
USD 159.00
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OVERVIEW There are currently more questions than answers on the subject of the legalization of medical and recreational marijuana and how does medical marijuana affect the workplace. The debate of the ...
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CAPA: Corrective and Preventive Actions and Non-Conformance
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Online Webinar by
Training Doyens
OVERVIEW If you only fix the symptoms – what you see on the surface – the problem will almost certainly happen again, which will lead you to fix it, again, and again, and again. If, instead, you look ...
Online
USD 199.00
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OVERVIEW If you only fix the symptoms – what you see on the surface – the problem will almost certainly happen again, which will lead you to fix it, again, and again, and again. If, instead, you look ...
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21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
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Online Webinar by
Training Doyens
OVERVIEW The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part ...
Online
USD 159.00
0 like
OVERVIEW The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part ...
MORE INFO
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GMPs Applied to Medical Cannabis: All You Need to Know
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Online Webinar by
Training Doyens
OVERVIEW When we discuss growing, producing, and manufacturing medical cannabis, we must think of it as a medicine. Medicine by definition, it is a substance intended to assist you with a medical condition, ...
Online
USD 159.00
0 like
OVERVIEW When we discuss growing, producing, and manufacturing medical cannabis, we must think of it as a medicine. Medicine by definition, it is a substance intended to assist you with a medical condition, ...
MORE INFO
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Ensuring Your Site is Ready for an FDA Inspection
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Online Webinar by
Training Doyens
OVERVIEW Although an effective Quality Management System should always be inspection ready, many medical device companies make basic mistakes during FDA inspections leading to 483s and even warning letters. ...
Online
USD 159.00
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OVERVIEW Although an effective Quality Management System should always be inspection ready, many medical device companies make basic mistakes during FDA inspections leading to 483s and even warning letters. ...
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What You Need to Do to Prepare for a Successful Inspection
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Seminar by
GlobalCompliancePanel
Description: Senior management takes responsibility for Quality and GXP compliance. It is not something delegated to the Quality unit or to the Regulatory Affairs group. Developing and implementing an ...
fremont
USD 1,495.00
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Description: Senior management takes responsibility for Quality and GXP compliance. It is not something delegated to the Quality unit or to the Regulatory Affairs group. Developing and implementing an ...
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Human Error Reduction Techniques for Floor Supervisors
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Online Training by
247compliance
Supervision plays a crucial role in Human Error Reduction and Control. Critical Factors like preparation, planning, scheduling, and communication, among many others, will be discussed as part of this ...
Online
USD 199.00
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Supervision plays a crucial role in Human Error Reduction and Control. Critical Factors like preparation, planning, scheduling, and communication, among many others, will be discussed as part of this ...
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HIPAA Waivers during COVID-19
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Online Webinar by
Netzealous LLC - MentorHealth
Overview: This webinar will review the sections of the HIPAA privacy rule that under the federal emergency for COVID-19 declared in March will be under a waiver issued by the OCR and penalties will be ...
Online
USD 139.00
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Overview: This webinar will review the sections of the HIPAA privacy rule that under the federal emergency for COVID-19 declared in March will be under a waiver issued by the OCR and penalties will be ...
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2020 Trends Related to 21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
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Online Webinar by
Training Doyens
OVERVIEW The webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with FDA 21 CFR ...
Online
USD 159.00
0 like
OVERVIEW The webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with FDA 21 CFR ...
MORE INFO
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FDA Scrutiny of Promotion and Advertising Practices
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Seminar by
GlobalCompliancePanel
If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue. Advertising and promotion for devices is weak and lacks legal clarity. For drugs, the regulations ...
fremont
USD 2,000.00
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If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue. Advertising and promotion for devices is weak and lacks legal clarity. For drugs, the regulations ...
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How can companies allocate scarce resources
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Training by
Compliance4All
Overview: This webinar will help you understand the critical ingredients for conducting an effective root cause analysis, also you will learn how to Analyze and document the root cause of the problem. ...
Fremont
USD 150.00
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Overview: This webinar will help you understand the critical ingredients for conducting an effective root cause analysis, also you will learn how to Analyze and document the root cause of the problem. ...
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Industrial Technical Trainer Certification
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Seminar by
GlobalCompliancePanel
Course "Industrial Technical Trainer Certification" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Each ...
fremont
USD 1,295.00
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Course "Industrial Technical Trainer Certification" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Each ...
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6-Hour Virtual Seminar on Biostatistics for the Non-Statistician
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Online Webinar by
GlobalCompliancePanel
Statistics is a useful decision making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on development of a drug or procedure, it is imperative ...
Online
USD 545.00
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Statistics is a useful decision making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on development of a drug or procedure, it is imperative ...
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6-Hour Virtual Seminar - Batch Record Review and Product Release
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Online Webinar by
GlobalCompliancePanel
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for ...
Online
USD 545.00
0 like
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for ...
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