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Training Services - pharmareg

Pharma Reg
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Pharma Reg
Pharma Reg
Our training philosophy

Expert knowledge and real-life case studies are combined to form an ideal learning experience. Professionals from industry, academia and regulatory authorities provide the lectures.

Our expert trainers use their vast experience to educate on the importance of GMP/GDP, why you should strive for continuous improvement and how you can apply our theory to practice.

TRAINING
Who should register?
If you are working in the pharmaceutical, biotech or related industries these training courses are extremely beneficial. From operators, quality assurance staff and lab technicians to CEO's; we have a training that matches your learning goals.

Most Popular In-House Training
Good Manufacturing Practices (GMP Basics & Expert)
Good Distribution Practices (GDP Basics & Expert)
Data Integrity
Human Error Reduction
Auditing & Self Inspections
Risk Management
Train the Trainer

CERTIFICATE
In-House GMP & GDP Training
Pharma Reg has 32 of experience in providing training to GMP and GDP regulated organizations. This includes manufacturers, distributors, laboratories, hospitals, pharmacies and related industries. An advantage of our in-house training courses is that the program, training content, workshops, exercises and methodology can be adapted to suit the specific needs of your company.

GMP & GDP Auditing Training
Auditing (Inspection) of suppliers is a GMP & GDP requirement. PCS has a number of auditing courses which can be provided in-house. Pharma Reg can focus on your specific GMP & GDP Auditing procedures and/or policies.

Quality Management Systems

Quality Management systems are difficult to implement, maintain or upgrade. Pharma Reg  has a number of courses aimed at specific parts of a QMS which can be adapted to focus on your own Quality System.

Internal & External Auditing
Advanced Auditing Techniques
FDA Inspection Preparedness
Auditing QC Laboratories
Auditing Aseptic Laboratories
Auditing API / Excipient Suppliers
Auditing Computerised Systemsa

Production Process

The production process is the most important element within every pharmaceutical company. To retain control of this process is essential to adhering to GMP & GDP regulations. These PCS courses are designed to assist your company in controlling, upgrading and assessing your production processes.

Packaging
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Aseptic Production
Environmental Monitoring
Disinfection and Sterilisation
Process Validation
Risk Analysis of Production Processes
Hygiene for Production Personnel
Microbiology for Non-Microbiologists
Cleaning Validation
HACCP
FMEA
Principles of Contamination Control
Critical to Quality Parameters (CQP)
Critical to Quality Attributes (CQA)

General GXP Courses

The following courses do not apply to a specific category but are designed to offer participants different levels of GMP & GDP related training. Process operators might benefit from a GMP Basic Course while upper management may benefit from a Quality Culture training or GMP Update seminar.

GMP - the Basics
GMP for Process Operators
GMP for Mid-Level Management
GMP for Upper Management
GMP Awareness
Quality Culture
Annual GMP Update 2022
Good Distribution Practices (GMP)
GMP for Biotechnological Products
GMP - For the Entire Organization

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