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Good Manufacturing and Laboratory Practices Workshop for Pharmaceutical, Biotech, and Medical Devices Professionals
Session 1: 27 - 28 March 2025
Session 2: 3 - 4 April 2025
This workshop provides an in-depth understanding of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices) for the Pharmaceutical, Biotech, and Medical Device industries. This hands-on training focuses on operational aspects and strategies required for seamless transition from R&D to GMP-compliant manufacturing.
Topics covered include scaling up, operational risk management, deviation handling, and CAPA implementation, documentation, and quality systems integration. With experienced speakers from SeerPharma, practical case studies and real-world problem-solving, this workshop will enable professionals in manufacturing, quality assurance, and regulatory affairs to successfully implement and manage operational controls, ensuring the integrity of product quality across manufacturing and lab environments.
| Category | Registration Fees* |
Early Bird Fees
12 February - 9 March | SGD 1200 |
Normal Fees
10 March - 17 March | SGD 1500 |
| * All Fees exclude GST |
REFUND POLICY
All request for withdrawal must be received 2 Weeks before the start of the workshop for the course. Late withdrawals will be subjected to payment of the FULL course.
CoRE is an accredited provider and continuing education credits are available for pharmacists through the Singapore Pharmacy Council (SPC).
Attendees who wish to avail of these credits are required to sign the relevant registration form along with their CPE number. The attendee’s details will be submitted to SPC after the event and credited upon SPC’s approval.
Date and Time
27 Mar 2025 @ 00:00 - 04 Apr 2025 @ 00:00