Our services

SeerPharma provides fully integrated solutions across QA, GxP compliance, training, risk management, validation, IT, productivity and quality management systems. Our solutions service the entire product lifecycle, from pre-clinical to commercial manufacture.

We offer international quality management and cGMP experience and practical advice to support client’s compliance management and productivity improvement across the pharmaceutical, medical device and biological industries.

Depending on client needs such as business criticality, time, or budget, we can provide senior consulting expertise and managed resources to provide the optimum solution.

Our integrated professional services, training and technical solutions meet all international regulatory standards including FDA, EU, PIC/S, TGA, ISO, ICH, and WHO.

SeerPharma's Capability Statement

Managed contract resources
SeerPharma provides managed contract resources in validation, technical writing, protocol writing, IT, and compliance support. Click here to find out more.

GeneEd therapeutic web-based training
SeerPharma partners with GeneEd to now distribute courses in Major Therapeutic Areas, Clinical Research, and Biotechnology & Genetics.

New training initiatives
MTAA medical devices e-learning
SIA laboratory practices e-learning
Bradford University/MDIS Singapore cGMP courses

Good Clinical Practices
SeerPharma teams with Evado to market its clinical management software.

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