Singapore Public Training

SeerPharma (Singapore) Pte Ltd has developed new GxP Master Development Training Program on various subjects.  Courses are held in Singapore.

For more information and to register click a course title below.

• 21 - June 2012 Good (Quality Control) Laboratory Practices (G(QC)LPs): Strengthening Analytical Credibility to Reduce the Cost of Compliance
• 12 - 13 July 2012 Contamination Control: Idendifying and Reducing Contamination Risks for Pharmaceutical Products using risk-based Methodologies
• 02 - 03 August 2012 Aseptic Biopharmaceutical Manufacturing:  Meeting the Expectations of the International Regulations and Improving Compliance of your Facilities, Equipment, Utilities and Processes
• 30 - 31 August 2012 Good Distribution Practices: Reducing your Regulatory Costs through Effective GDP Implementation
• 27 - 28 September 2012 Process Validation Essentials: Contemporary Process Validation, its not just three batches
• 18 -19 October 2012 Solid Dose Manufacture Principles and Practices: Develop Knowledge and Aquire an Understanding of Formulation, Scale-up and Optimisation of Finished Dose Forms
• 08 - 09 November 2012 Good Laboratory Practices – Non Clincal Studies: Doing Things Right for Cost Effective Drug Development and Global Registration
• 06 - 07 December 2012 Internal Quality Audit: Improving your Business and Regulatory Performance through an Effective IQA Programme

Contact Details

Denise Collyer

Tel: +65 6774 5800 Fax: +65 6774 6800
E-mail: training@seerpharma.com

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