PG DIPLOMA -FULL-TIME & PART-TIME

PHARMACEUTICAL AND BIOTECHNOLOGY ADVANCED DIPLOMA

PROGRAM DESCRIPTION

This comprehensive postgraduate diploma program has been designed to meet the requirement and demands of the industrial standards set by potential employers. It covers a wide range of pharmaceutical and biotechnological skill development in QA, QC, R&D, formulation, technology transfer, validation and regulatory affairs.

Regulatory affairs clinical science pharmacovigilence clinical trial monitoring audits and inspections ethics & human protection.

Full-time: 48 weeks    Part-time: 116 weeks

  • Optional Job Assistance for co-op, internship and full-time opportunities within pharmaceutical and bio-pharmaceutical and related sectors

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More than 18 years old, Science or Engineering or Equivalent

  • Good Manufacturing & Good Clinical Practices
  • Introduction to Laboratory Testing & GLP
  • Dissolution & Hands-on Training
  • High-Performance Liquid Chromatography (HPLC)
  • Gas Chromatography (GC)
  • HPLC & UV for Dissolution: Method Development & Method Validation
  • GC & UV Spectrometer: Method Development & Method Validation
  • Pharmaceutical and Biotechnology Formulation & Validation Technology
  • Collective Validation
  • Cleaning & Sterile Validation
  • Packaging Validation & Packaging Components
  • Process Validation
  • Introduction to Regulatory Affairs
  • Professional Regulatory Affairs
  • Introduction to Clinical Studies
  • Scientific Technical Writing

Quality Control and Quality Assurance Area:

Technologists, Raw Material Chemists, Finish Product Chemists, Stability Chemists, R&D Chemists, Scientists, Calibration Chemists, Document Reviewers, Laboratory Coordinators, Trainers, SOP Writers, Auditors, Supervisors, and Managers.


Formulation Area:

Laboratory Coordinators, Formulation Technicians, Production Operators, Formulation Scientists and Formulation Managers/Directors.


Technology Transfer Area:

Validation Assistants, Process Development Scientists, Technology Transfer Specialists, Technology Transfer Coordinators and Document Coordinators.


Validation Area:

Process Validation Scientists, IQ/OQ/PQ Specialists, Cleaning Validation Specialists, Packaging Validation Specialists, Thermal Validation Specialists, Computer Validation Specialists and Validation Managers.


Regulatory Affairs Area:

Regulatory Affairs Associates, Reviewers, Auditors, and Managers/Supervisors/Directors.


Clinical Research Area:

Clinical Research Scientists, Clinical Research Organizers /Associates, Managers/ Supervisors/Directors. Regulatory Affairs Area: Regulatory Affairs Associates, Auditors, and Regulatory Affairs Managers/Supervisors/Directors.

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Testimonials

  • Robert Bess, B.Sc.

    Production Technician, Apotex Inc.

    NACPT helped me enormously and I shall be eternally grateful.

  • Dr.Taiwo Sonoiki

    Clinical Assistant

    For new immigrants like myself, the difficulty in obtaining Canadian references proves to be an important challenge.

  • Lorrein Muiruri, BSc., from UofT

    Clinical research Assistant, Inflamax Research Inc

    Lorem Ipsum is simply dummy text of the printing and simply dummy text of the typesetting industry.