Regulatory Compliance Training, Standards and Best Practices...Get educated on regulations affecting your industry and listen to experts on best practices to streamline quality and compliance processes and meet the regulatory demands with these new courses through LatitudeLearning partner ComplianceOnline:

- Effective Training for FDA Compliance: What to train - How much to Train - How to Document Effectiveness
- Introduction to Good Documentation Practices for FDA-Regulated Industries
- Risk-Based Verification and Validation Planning to Meet US FDA and ISO 13485 Requirements
- Designing an Effective and Efficient Internal Audit Process for Your Quality Management System
- FDA Inspections-Dos & Don'ts
- Review of Changes to the New ANSI-AAMI-ISO 11137-2006 (Parts 1, 2, & 3) Sterilization of health care products - requirements for validation and routine control - Radiation Sterilization
- Medical Device Complaints, M's and Recalls
- Ethylene Oxide (EO) Sterilization of Medical Products: The Basics
- Good Laboratory Practice Regulations
- Statistical Sampling Plans for Audits
- CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process
- Understanding the new International and FDA accepted Software Development Standard IEC 62304
- Supplier Evaluation and Assessment Program: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-effective Manner
- Process-Based and Metric-iven Internal Audit Approach
- Integrating Risk Management with the CAPA process
- Effective Internal Quality Audit: Identifying Corrective and Preventive Actions
- Transfer of Analytical Methods and Procedures:FDA Requirements and Strategies and Tools for Implementation
- Medical Devices in the EU: CE Mark and 93-42-EEC Directive
- Bullet-Proof CAPA
- Utilizing ICH Guidelines for GCP Regulatory Compliance
- Human Factors Standards and Guidances for Medical Devices -- which documents apply to my situation?
- Conducting Successful Product Complaint Investigations
- Risk-Based Equipment Validation
- 510(k) Applications made Simple
- Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices
- Important requirements when validating sterilizing grade filters
- A Practical Approach to Microbial Data Deviation Investigations
- Residual Solvent Analysis According to USP <467> - Understanding and implementing the new USP chapter
- Environmental Monitoring and the Contamination Control Plan
- Effective Training Practices for FDA Compliance
- Basics of testing associated with sterilization validation and routine processing
- Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities
- Laboratory Investigations Relating to Sample Re-Analysis: Covering the basics before being called out
- FDA's New Supply Chain Safety Initiative: Quality Control and Legal Ramifications for Drug, Device, and Biologic - Manufacturers and Their Suppliers
- You have a sterility or Bioburden test failure - Now what?
- Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs
- FDA 21 CFR Part 11 for techies
- FDA Warning Letter - Consent Decree Software Validation
- FDA Warning Letter Closeout Program
- Conducting a risk assessment for objectionable microorganisms
- Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11
- Lawful Pre-FDA Approval & Pre-FDA Clearance Communication
- Understanding Disinfectant Qualification Studies How to avoid errors
- What exactly is required for 21 CFR Part 11 compliance?
- Excel Spreadsheets - Develop and Validate to Eliminate 483s