Pharmaceutical Quality Assurance and Regulatory Compliance
Key Details
Virtual Certificated Programme
Live Online Classroom
24th – 26th February 2025
Overview
Pharmaceutical Quality Assurance and Regulatory Compliance
The pharmaceutical industry operates within complex and highly structured regulatory frameworks designed to ensure product quality and patient safety are at its core. However, regulatory requirements often evolve in response to emerging risks, scientific advancements, and changing societal expectations. Keeping pace with these updates is a constant challenge for pharmaceutical companies to respond and comply.
For pharmaceutical organisations to maintain high standards, they must implement robust good manufacturing practice to comply with regulatory standards across jurisdictions. Good manufacturing practice must be embedded within an organisation at all levels, with employee buy-in and compliance well established throughout. Failure in any of these areas could lead to patient-safety risks, product recalls, legal penalties and even loss of market access.
This three-day training programme has been designed to establish and maintain organisation-wide good manufacturing practice and compliance. Throughout the course, participants will analyse EMA, MHRA and FDA regulatory standards, examine how to create a culture of compliance, and evaluate best practice in the control of materials and suppliers, manufacturing, and how to prepare for a GMP inspection. By the end of the course, participants will have a strong understanding of quality assurance and quality control across pharmaceutical production as well as how to implement effective change and improvements in their organisation.
Benefits
This programme is a comprehensive exploration of pharmaceutical quality and regulatory compliance through immersive and thought-provoking lessons to ensure both you and your organisation benefit from the training, including:
Programme Content
Key Topics:
Full Programme:
To access the full programme and details, please complete the following form.
The course is designed for:
- Those in the pharmaceutical industry with responsibility over:
- Compliance
- Quality Assurance
- Quality Control
- Production Management
- Safety
- Engineering
- Oversight and management of pharmaceuticals
What to expect:
This live, virtual training programme is designed to create a highly engaging, dynamic and varied learning environment through:
Why the International Centre for Governance and Policy?
Creating the Policy Makers, Regulators, Parliamentarians, Diplomats, and Public Officials of the Future
The International Centre for Governance and Policy is a specialist training and consultancy organisation which provides leading programmes and interventions for governments, public authorities, private entities and non-governmental organisations all over the world.
With a firm belief that good governance structures and effective policy processes enable any organisation to deliver for their stakeholders and remain accountable to those they serve, the Centre delivers world-class training programmes based on the latest research, innovations and citizen-focused outcomes.
Trainers
Meet the Trainers and Experts involved in your professional development:
Fees and Requirements
Tuition fee: GBP £1,750
Fees include access to the training via online learning software, tuition materials, workbook and networking opportunities. You will be awarded a certificate of completion from ICGP at the end of the course.
To find out more about this course, please click register now: