SeerPharma Pty Ltd :: DISCover web-based training

Modules available

Click on one of the module series below to see more information about our regulatory and compliance modules.

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GMP Series

QC Series

IS/IT Series

Medical Devices Series

Validation Series

Lab Series (ISO17025)

SeerPharma has partnered with Intellego to distribute their suite of drug development, registration, and clinical trials.


Intellego web-based training

ESS01 Essentials of EU and US Regulatory Affairs for Human Medicinal Products SUB01 Orphan Drug Applications in the EU and USA SUB02 The European Centralised Procedure (CP) SUB03 The Mutual Recognition Procedure (MRP) SUB04 Preparing Submissions in the Common Technical Document (CTD) Format SUB05 Electronic Common Technical Document (eCTD) SUB06 EU Variations Procedure SUB07 Registration of Monoclonal Antibodies SUB08 The ANDA: Requirements for Obtaining FDA Approval for Generic Product in the USA SUB09 The NDA Process: Requirements for Obtaining Approval for a New Drug in the USA SUB11 The Decentralised Procedure (DCP) PV01 An Introduction to Pharmacovigilance (PV)		CT01 How to Obtain Approval to Conduct Clinical Trials in the EU CT03 An Introduction to ICH Good Clinical Practice (ICH-GCP) CT04 An Introduction to Clinical Trial Preparation and Design CT05 An Introduction to Clinical Trials in India CT06 Clinical Trial Monitoring: Site Evaluation and Set-up CT07 Introduction to Clinical Trials and Drug Development CT08 Clinical Trial Monitoring: Study Monitoring, Documentation and Closure CT09 Preparing for a GCP Audit or Inspection CT10 The IND: How to Gain Approval for Clinical Trials in the USA SC01 Pharmacokinetics and Pharmacodynamics in Drug Registration GXP01 An Introduction to Good Manufacturing Practice (GMP) for Drug Products