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Laboratory & Medical Auditing
Find training in the area of Laboratory & Medical Auditing in the list of courses below.

You will find a range of courses that you can search amongst and then use our filters to refine your search to get more specific results.
Courses (66)
Providers (16)
Displaying 1-20 of 66 results
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Auditing to Pharmaceutical Standards
Recommended
5.0 (1)
Reading Scientific Services Ltd
It is a regulatory requirement for organisations within the Pharmaceutical and Allied Industries to audit active pharmaceutical ingredient (API) manufacturers,...
  • From 695 GBP
  • Cheshire
Medical Device Single Audit Program Implementation
5.0 (1)
Lloyd's Register
This two-day Medical Device Single Audit Program (MDSAP) Implementation course is for medical device manufacturers who want to be audited...
  • From 1,290 GBP
  • Multiple (2)
Medical Device Regulatory Requirements - (5 course bundle)
NSF International, Pharmaceutical Services
Bundle of 5 Courses - Medical Devices Regulatory Requirements. United States, Japan, Australia, Brazil, Canada A comprehensive overview of each...
  • From 1,400 USD
  • Distance
Implementation of the Medical Device Regulation (MDR)
5.0 (1)
Lloyd's Register
Lloyd’s Register has developed this two-day course for enterprises who already manufacture medical devices against the existing Medical Device Directive...
  • From 1,548 GBP
  • Multiple (3)
FDA Medical Device Reporting (MDR)
NSF International, Pharmaceutical Services
Medical Device Reporting is part of the Code of Federal Regulations - 21 CFR Part 803, mandated by Congress in...
  • From 299 USD
  • Distance
Introduction to the Medical Device Regulation (MDR)
Lloyd's Register
This course provides an overview of the structure and revised scope of the Medical Device Regulation (MDR) for you to...
  • From 930 GBP
  • Multiple (3)
CQI IRCA ISO 13485:2016 Internal Auditor Training Course
Batalas Ltd
This ISO internal auditor training course equips delegates with the skills and knowledge to conduct internal audits to ISO 13485....
  • Nationwide
European Union Medical Device Regulation – EU MDR
NSF International, Pharmaceutical Services
In 2017, the Medical Device Regulation (EU MDR) 2017/745 was published, introducing major changes to the previous Medical Device Directive...
  • From 399 USD
  • Distance
Medical Device Complaint Handling and Servicing
NSF International, Pharmaceutical Services
Maintaining proper Complaint files is an essential element of the medical device quality management system. This course will examine the...
  • From 300 USD
  • Distance
Design Controls for Medical Devices and IVDs
NSF International, Pharmaceutical Services
NSF International’s web-based virtual training course provides a basic understanding of Design Controls for medical devices and IVDs. Providing knowledge...
  • From 199 USD
  • Distance
CQI IRCA ISO 13485:2016 Internal Auditor Training Course
4.6 (12)
Batalas Ltd
This ISO internal auditor training course equips delegates with the skills and knowledge to conduct internal audits to ISO 13485....
  • From 945 GBP
  • Multiple (2)
Auditing to Pharmaceutical Standards
5.0 (1)
Reading Scientific Services Ltd
It is a regulatory requirement for organisations within the Pharmaceutical and Allied Industries to audit active pharmaceutical ingredient (API) manufacturers,...
  • From 695 GBP
  • Cheshire
Active Pharmaceutical Ingredients Auditing
5.0 (1)
Reading Scientific Services Ltd
This Active Pharmaceutical Ingredients Auditing course provides the knowledge base and skills to enable effective auditing and reporting of audits...
  • From 695 GBP
  • Reading
ISO 13485:2016 – International Medical Device QMS Standard
NSF International, Pharmaceutical Services
This course provides in-depth instruction and expert clarification of ISO 13485:2016, the standard which serves as a basis for many...
  • From 399 USD
  • Distance
Pharmaceutical Practical Auditing Skills
4.3 (3)
Reading Scientific Services Ltd
This course provides an introduction to the requirements of internal auditing described in the international standard ISO 19011. Frequent opportunities...
  • From 1,390 GBP
  • Multiple (2)
MDR Implementation
Lloyd's Register
Lloyd’s Register has developed this two-day course for enterprises who already manufacture medical devices against the existing Medical Device Directive...
  • Nationwide
Introduction to the New IVDR
Lloyd's Register
As a forward-looking manufacturer operating in the highly regulated and high stakes world of medical devices manufacturing, you want to...
  • Nationwide
CQI IRCA ISO 13485:2016 Foundation Training Course
Batalas Ltd
CQI IRCA Certified ISO 13485:2016 Foundation Training Course - Quality Assurance and Auditing - Open Course  This highly interactive 1...
  • Nationwide
Pharmaceutical GMP Audits and Self-Inspections
5.0 (3)
NSF International, Pharmaceutical Services
NSF’s five-day lead auditor training course is designed and developed by ex-MHRA inspectors and industry experts. One of the most...
  • From 3,040 GBP
  • Multiple (5)
CQI IRCA ISO 13485:2016 Foundation Training Course
5.0 (3)
Batalas Ltd
CQI IRCA Certified ISO 13485:2016 Foundation Training Course - Quality Assurance and Auditing - Open Course  This highly interactive 1...
  • From 445 GBP
  • Multiple (2)
ISO 14971 Risk Implementation
Lloyd's Register
This three-day course from Lloyd’s Register offers practical insight in implementing the requirements in ISO 14971. It will provide you...
  • Nationwide
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