GMP & Quality Training
ERA (Excellence in Regulatory Affairs) offers
comprehensive GMP (Good Manufacturing Practices)
and Quality Training programs designed for Pharmacy,
Life Science graduates and pharmaceutical professionals.
Our training provides practical knowledge of quality
systems, manufacturing compliance, documentation
practices and regulatory requirements followed in
the pharmaceutical industry.
The program is structured to help participants
understand the principles of pharmaceutical quality,
regulatory compliance and Good Manufacturing Practices
essential for maintaining product quality, patient
safety and regulatory compliance. Through practical
examples and industry-oriented learning, students
develop skills required for successful careers in
Quality Assurance (QA), Quality Control (QC) and
pharmaceutical manufacturing.
Training Program Highlights:
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Introduction to GMP –
Understanding the fundamentals of Good
Manufacturing Practices and pharmaceutical
compliance requirements.
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Quality Assurance (QA) –
Training on quality systems, compliance
monitoring, documentation control and
regulatory expectations.
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Quality Control (QC) –
Overview of laboratory operations,
analytical testing and quality evaluation
procedures.
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Good Documentation Practices (GDP) –
Proper documentation techniques, record
maintenance and data integrity principles.
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Validation & Qualification Concepts –
Introduction to process validation,
equipment qualification and quality
management systems.
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Deviation, CAPA & Change Control –
Understanding deviation management,
corrective and preventive actions (CAPA)
and change control procedures.
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Audit & Compliance Management –
Basics of GMP audits, inspection readiness
and compliance monitoring.
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Career Guidance & Industry Exposure –
Practical insights and career development
support for QA, QC and manufacturing roles
in the pharmaceutical industry.