Classroom Training Services for Pharmaceutical and Medical Device Industry
One of the major benefits of our classroom training is the option for individual registration, allowing personalized learning. Our courses focus on making theory practical through interactive discussions and case studies, encouraging the exchange of insights and best practices from different companies within the industry.
Our trainers at Rescop Academy maintain a strong connection to current industry practices by combining training with consultancy assignments. This approach ensures that all training materials reflect the latest developments and regulatory standards.
Available Classroom Training Courses
- GAMP 5 Training: Explore the Good Automated Manufacturing Practice framework, a widely accepted set of guidelines in the industry.
- GxP Data Integrity Training: Understand the critical aspects of data integrity in Good Practice (GxP) compliance.
- GxP Training: Comprehensive training covering the essential aspects of GxP compliance in pharmaceuticals and medical devices.
- Life Cycle Process Validation Training: Learn how to apply the validation lifecycle approach to ensure product quality.
- ISO 13485 Training: Gain in-depth knowledge of ISO 13485, the international standard for medical device quality management systems.
- Permanent Inspection Readiness Training: Prepare your organization for continuous inspection readiness and regulatory audits.
- Quality Management Training: Enhance your skills in quality management systems and best practices within the life sciences sector.
- Spreadsheet Validation Training: Learn effective methods for spreadsheet validation and ensure regulatory compliance.
- Validation Using Agile Training: Explore how to incorporate Agile methodologies in the validation process for a more efficient approach.
Stay up-to-date with Rescop Academy’s interactive workshops and hands-on training to keep ahead of industry regulatory compliance and quality standards.