SCOPE
This one day refresher course offers a practical evaluation of the key roles and responsibilities of the Responsible Person (RP) and Deputy RP in the light of the extensive requirements included in the MHRA Orange/Green Guides in relation to current Good Distribution Practice (GDP) as required by Directive 2001/83/EC, Directive 2004/27/EC and the EU Guidelines on Good Distribution of Medicinal Products for Human Use 2013/C 343/01. In particular it gives you the opportunity to share best practice and experiences in an open learning environment.
SUITABILITY
The refresher course is aimed at RP鈥檚 and Deputy RP鈥檚 who have already undertaken initial RP training but who need to keep updated with current regulations and expectations of the competent authorities for Continuing Professional Development (CPD). Note, it is not a suitable alternative for those who have yet to undergo initial RP training.
This 鈥榰pdate鈥� course would also benefit quality managers, and personnel in regulatory, compliance, distribution, warehousing, supply chain management and customer service who need to appreciate the implications of the changes. It is designed for all those who need to understand the revised key GDP quality components necessary to operate as a holder of an MHRA or EU.
Section 2.4 of Directive 2013/C 343/01 states that RPs should receive regular training to maintain their competence in GDP, this course is designed to meet this need.
LEARNING OUTCOMES
The refresher course is a highly interactive 鈥榟ands on鈥� learning experience; breakout sessions will review the most recent examples of deficiencies found by regulators and how to address and improve compliance in these critical areas.
By the end of the course you will:
- Be familiar with the 2013 GDP requirements as covered by EU directives/regulations and guidelines (including the 鈥極range Guide鈥�).
- Understand the full breadth of your responsibilities and accountabilities as defined under the RP Gold Standard with a clear focus on the increased legal and compliance responsibilities.
- Have a comprehensive understanding of the 鈥榟ot topics鈥� from regulators and recent regulatory updates including the latest MHRA symposium.
