Are you looking for online training for Medical Device Industries and Life Sciences? What all it has –
- 60 minutes of online training
- Convenient access anytime, anywhere
- A great way to meet your educational needs
- Courses for the Life Sciences and Medical Device Industries
Check out here –
- Basic Requirements for Steam Sterilizer Validation per ISO 17665
- Best Practices for Managing FDA Investigators and Handling FDA 483 Observations
- Medical Device Complaints, MDR’s and Recalls
- Six Sigma Methodology for Process Validation
- Documenting a Risk-Based Quality System – for Compliance and Cost-Savings
- How to perform effective supplier audits, and avoid FDA 483’s and Warning letters
- Verification vs. Validation in Regulated Industries
- CAPA Essentials – core principles and practices needed to implement an effective and efficient CAPA process
- Introduction to Process Capability (Cp, CpK, Pp, Ppk)
- How to Use the System Risk Level to Save Time and Money on Computer System Validations
- Implementing the new International and FDA accepted Software Development Standard IEC 62304
- Risk Management Activities during Design Input
- Developing a Robust CAPA System
- Complying with 21CFR Part 11-Understanding the Role of Predicate Rules
- The New Dietary Supplement Good Manufacturing Practices
- Configuration Management and Change Control for Computer Systems
- Cleanroom Operation, Maintenance and Operators
- Conducting and Documenting Proper Risk Analysis In compliance with ISO 14971
- 510(k) Preparation for a Small to Medium-Sized Company
- Applying Lean Documents to a Project – how to create a project file, follow design controls, yet maintain a lean set of project documents.