Training

Online training

Our online training is provided via our training partners, click here to view our online training packages.

Public courses

Our training is used by the pharmaceutical industry worldwide to comply with regulatory expectations and maximize the contribution of their staff at all levels.

Delegates leave our courses:

  • better informed about the subject area
  • better aware of their role and impact upon product quality and/or regulatory compliance
  • better motivated to improve their contribution

All our courses are designed to be informative, involving, participative, relevant and, above all, enjoyable.

We achieve this by:

  • presenting lectures and tutorials which are clear and focused
  • supporting what we say with illustrations from experience in the industry
  • using clear visual aids which enhance the message
  • allowing ample time for discussion with delegates – during presentations as well as after
  • promoting understanding and involvement of all attendees via the use of interactive sessions such as teamwork tasks and workshops.

Many of our training courses can if required  prepare delegates for the examinations for Professional qualifications with the Chartered quality Institute and are recognized as part of your Continued Professional development . Our commitment to the client and the delegates does not end when the course finishes. We encourage companies and individuals to contact us if they feel we can assist with explaining issues further, problem solving, guidance on where to find relevant documents, further reading and so on.

On Site Training

On -Site training represents a significant part of our activities. Whilst some of these courses are based upon our public training courses, all courses are specifically designed to meet the client companies precise needs .On- site training courses can vary in duration from half a day up to five days.

We strongly believe that training is most effective when it is directly relevant to the activities performed by the attendees. With that in mind, we like to work closely with you to design courses which your staff can immediately relate to and which answer their specific questions.

Selection of training topics covered in recent Courses:

  • Supplier Audit of Active Pharmaceutical Ingredients and major Excipients
  • Audits/Self-Inspections for GxP compliance
  • Regulations for manufacture of Investigational Medicinal Products .
  • Implementing Continuous improvement and effective Change Control
  • Audit of Contract Manufacture and Testing
  • Monitoring Product and Process Deviation Reporting
  • Preparing CTD dossier for regulatory submission
  • Preparing for Regulatory  Inspections
  • Achieving Good Distribution Practice for Logistics/Warehousing
  • Good Clinical Practice in Clinical Trails
  • Business management administration for the Pharmaceutical Industry
  • Clinical Trials Packaging best practice
  • Quality Control
  • Role and duties of the Qualified Person
  • Implementing Pharmaceutical Quality Management Systems- ICH 10
  • Effective Quality by design in Product Development on a limited budget.
  • Regulatory Issues/Pharmaceutical Law for Pharmaceutical Manufacturing
  • Implementing Risk Management for Pharmaceutical Manufacture
  • Impact of   Stability Testing on Product specification .
  • Supplier Assurance Risk assessment.
  • Process control (PAT) and system Validation.