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Our purpose is to provide you with technical knowledge in an efficient, accurate and organized manner for the development of your abilities and skills.

We develop content and exclusive innovative solutions according to the specific needs of your company. The modality of the courses can be face-to-face, on-site, online, open or closed.

All our programs are based on a productive and quality approach through the use of tools such as:


The main courses offered by specialty area are:

  • Quality Manual Design
  • Design, Development and Implementation of Quality Systems ISO 9001/2015
  • Good Documentation Practices
  • Quality Risk Management

  • Qualification of Suppliers
  • Quality Agreement Management
  • Supplier Audit
  • Engineering and Automation
  • Commissioning
  • Productive Recipe Design (Equipment)
  • Design of Preventive Maintenance Plans
  • Critical Systems Qualification 
  • Productive Equipment Qualification 
  • Control Strategy Design
  • Process Validation and Cleaning Validation 
  • Development and Validation of Analytical Methods
  • Master Plans 
  • Critical Systems Qualification 
  • Productive Equipment Qualification 
  • Laboratory Equipment Qualification 
  • Qualification of Temperature Controlled Chambers 
  • Software Qualification 
  • Continuous Verification (Sustaining Qualified Status)
  • Process Transfer
  • Cleaning Validation 
  • Process Validation
  • Continuous Process Monitoring
  • CSV (Computer System Validation)
  • Good manufacturing practices 
  • Normative Operating Procedures
  • Root Cause Investigation 
  • Implementation of Control Strategies
  • Statistical process control 
  • Inspection and Sampling
  • Process mapping
  • Continuous improvement
  • Identification, Control and Improvement of Indicators
  • Preventive and Corrective Maintenance 
  • Design of Corrective Maintenance Plans
  • Preventive Maintenance Administration
  • Good Engineering and Automation Practices 
  • Productive Recipe Design (Equipment) 
  • Commissioning
  • Energy saving
  • Master plan
  • Risk analysis
  • Documentary Decommissioning of Equipment 
  • Releasing Strategy
  • Product Discontinuation
  • Coordination of Decommissioning and Discontinuation activities 
  • Disconnection and Packing of Equipment
  • Sampling and Chemical Analysis for Release
  • Development and Validation of Methods for Analysis of Products in Process
  • Development and Validation of Methods for Finished Product 
  • Development and Validation of Methods for Products in Stability Study 
  • Forced Degradation Study
  • Development of Microbiological Methods
  • Analytical Method Transfer
  • Resolution of Analytical Physicochemical and Microbiological Problems
  • Good Laboratory Practices 
  • Out of Spec Investigations
  • Laboratory Equipment Qualification
  • Physicochemical Analysis 
  • Microbiological analysis
  • Transportation Qualification
  • Warehouse Mapping
  • Good Storage and Distribution Practices


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