Pharmaceutical Product Development
An overview of current activities in genomics, in their translation into new drug discovery and the delivery of personalized medicine.
Biopharmaceutical Development (GMP)
This course will demonstrate that Biopharmaceutical manufacturing processes are highly product specific and almost always designed to fit the Biopharmaceutical molecule and provides the delegate with the following skills.
Quality Management System
The six Quality management courses provide14 hrs. of Continuing Education for your CPD and describes the Skills and competencies to provide you with the basis for managing and controlling quality.
Regulatory Affairs
This module is an introduction to International regulatory requirements for Developing , Manufacturing and distributing medicines for Human use and provides a basis for Pharmaceutical Regulatory Affairs knowledge essential for all staff working in Health Care and the Pharmaceutical Industry
This course gives an overview about the legal background of Pharmacovigilance regulation, and will review the new regulations for Good Vigilance Practice, the PharmacoVigilance System, Master file, and the duties & responsibilities of the Qualified person (PhV).
This Development program provides the essential Certification in GCP competence for Clinical Investigation teams required by Sponsors organisations before starting Clinical Trails. The program consists of a eLearning lecture which is supported by tutorial webinars based on This ICH E6 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial
Medical Devices
An overview of the current medical device requirements expected by key regulatory authorities to achieve a marketing authorization.
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