Browse 87 Medical Laboratory / Technology courses in USA
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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, ...
MORE INFO
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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
0 like
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 ...
MORE INFO
ENDED
21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
ENDED
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
ENDED
GMPs Applied to Medical Cannabis: All You Need to Know
ENDED
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