Custom Training – Onsite or Offsite

TrainingsAt last, Exclusive Training Workshops designed especially for your needs! SS”R” Us is pleased to introduce Pharmaceutical, Medical Device and Biotechnology On-Site Training Workshops.

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Advantages of On-Site Pharmaceutical, Medical Device, and Biotechnology Training:

  • Save money on travel expenses for multiple employees. SS”R”Us is willing to train any group size on any topic at any location.
  • Affordable in-house training by an industry expert – pay only as needed as an alternative to maintaining an internal training staff.
  • Allow us to customize course objectives around company-specific needs

Scientific Solutions “R” Us prepares new hires and refresh current personnel anywhere in the product cycle, from discovery through commercialization anywhere in the world. Scientific Solutions “R”Us provides On-site pharmaceutical, medical device and biotechnology training for groups of 5 or more. Experience the same in-depth, quality content provided by industry-active Course Instructors in the convenience of your office. SS”R”Us signature Continued Support also available on-site!

-         ICH Q3D Guideline for Elemental Impurities
-         Microbiological Contamination Control
-         Basic Problem Solving
-         Basic Statistics/Introduction to Minitab
-         Implementing a Complaint-Handling and Recall Program
-         Conducting Regression Analysis
-         Process Validation Principles and Protocols
-         Data Collection and Gage R&R
-         Implementing Statistical Process Control
-         Optimizing Teams for Success
-         Potential Failure Mode and Effects Analysis
-         Understanding and Conducting Data Analysis
-         Understanding and Measuring Process Performance
-         Understanding and Performing Hypothesis Testing
-         Listening to the Voice of the Customer
-         ISO 9000 & Related Standards
-         Risk Management and Analysis for Manufacturing Processes
Quality Systems for Medical Devices:
-         FDA’s QSR and ISO 13485
Medical Device RA/QA 
-         Global Product Submissions: FDA and EU Directive Requirements [510(k), PMA, CE Mark]
-         Quality Systems for Medical Devices:
-         FDA’s QSR and ISO 13485
-         Supplier Quality Management: Designing and Implementing a Successful Program
 -        Implementing a Complaint-Handling and Recall Program
-         Risk Management and Analysis for Medical Devices
-         Implementing Design Control Requirements and Best Practices
-         Process Validation Principles and Protocols
-         Implementing CAPA Programs for the Medical Device Industry
-         Developing and Maintaining a Compliant Document Management System
 Laboratory/Quality Control/Quality Assurance
-         Root Cause Analysis for Life Science Investigations
-         Calibration Requirements and Equipment Controls for Medical Devices
-         Software Verification and Validation Requirements
-         Sterilization Planning for Medical Devices
-         Introduction to Process Validation
-         Course Combo: Implementing Design Control Requirements and Best Practices and Risk
-         Course Combo: Implementing CAPA Programs for the Medical Device Industry
-         Root Cause Analysis for Life Science Investigations
-         Global Product Submissions: FDA and EU Directive Requirements [510(k), PMA, CE Mark
Pharmaceutical RA/QA
-         Supplier Quality Management: Designing and Implementing a Successful Program
-         Root Cause Analysis for Life Science Investigations