Responsible Person and GDP Cogent Approved

Mastering the Role of the Responsible Person (RP) for Comprehensive GDP Training Led by Industry Experts

The Responsible Person (RP) plays a critical role in ensuring that medicinal products are transported, stored and delivered in compliance with Good Distribution Practice (GDP).  Given the complexities of this role, our training program equips delegates with essential knowledge and skills to navigate the complexities of this multifaceted role. 

 

With over 25 years' experience in delivering highly impactful GDP training, our three-day RP course is led by industry leaders including ex MHRA inspector Tony Orme and practicing RPs. It incorporates the latest regulatory updates and best practices and is proudly Cogent Gold Standard approved, assuring you that it meets the rigorous standards set out by the MHRA. 

 

 

Interested in RP training for your team? Contact us today. 

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Duration
3 days
CPD Hours
21 hrs
Locations
  • Online
  • Reading (RSSL)

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Who Should Attend 

This course is designed for people who are seeking to be named as a Responsible Person on a WDA and  is relevant for professionals involved in the procurement and sale of medicinal products, including WDA holders. It will also benefit supplier auditors, existing RPs looking to enhance their CPD and trainee/QPs looking to gain a deeper understanding of GDP and the RP responsibilities. 

Organisations applying for or holding a Wholesale Dealers Authorisation (WDA) must have a RP named on the license. The RP is responsible for ensuring compliance with GMP and understanding the legal responsibilities of holding a WDA license. This includes ensuring that all medicinal products in the legal supply chain are handled, transported, stored and distributed correctly 

 

Another core requirement of Good Distribution Practice is the need to have a well-designed Quality Management System (QMS) focused on compliance and continual improvement. The RP is legally required to ensure the QMS is implemented by maintaining oversite of its routine operation. This area will be covered in detail as it has been highlighted by the MHRA as the top area deficiencies are found during inspections. 

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Key topics

The course includes the following topics: 

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    Expectations to become a RP 

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    Role of the RP and key regulatory requirements e.g. MHRA 

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    What GDP covers and the license types 

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    The WDA(H) and how to apply 

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    License checks - Eudra GMDP & MHRA GMDP 

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    Key personnel in the supply chain and GDP 

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    Brexit 

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    Quality management and its tools 

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    Premises and equipment 

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    Documentation and Operations 

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    Complaints, returns, suspected falsified medicines and recalls 

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    Outsourced activities 

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    Self-inspection and regulatory inspections 

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    Transportation, containers, packing and labelling, products requiring special conditions 

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    Import and export 

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    Specific provisions for brokers 

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    Controlled drugs 

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    Specific provisions for the RP 

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    Responsibilities for the WDA holder 

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    Parallel distribution 

Learning Outcomes

Attending this course will ensure that you: 

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    Understand the role of the RP in personal responsibilities and patient/product user safety 

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    Understand the legislation and licensing requirements for wholesale distribution of medicinal products

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    Have a clear understanding of the competent authority’s role in licensing of wholesale dealing of medicines and enforcing GDP guidelines  

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    Understand the relevant role of national organisations that also regulate the supply chain of medicinal products 

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    Understand all aspects of the European Pharmaceutical directives and guidelines related to GDP and be aware of GMP

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    Understand and recognise best practice in GDP and why it is essential in maintaining the quality and integrity of medicinal products 

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    Appreciate how to implement an effective quality compliance system that can be maintained and improved 

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    Are able to identify a medicinal product, the different legal categories, storage conditions and Marketing Authorisation (MA) types  

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    Understand the importance of applying due diligence  and when to  report any suspicious events to senior management, the competent authority and the MA holder

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    Understand how to review the effectiveness of an organisation’s QMS and implement effective CAPAs

Meet your expert tutors

Learn from the best in the industry. Our diverse team of highly experienced subject matter experts are passionate about sharing their knowledge with you. 

David Abraham

David Abraham

With extensive knowledge of business operations and processes, manufacturing operations, logistics and pharmaceutical industry applications, David has operated in and alongside working parties at national and international level. Developing guidance and standards for the industry, David is held in high regard within the industry and has been instrumental in the development of the PS 9000 publications.
Tony Orme

Tony Orme

Now an independent consultant, Tony has 32 years' experience in the regulation of pharmaceuticals with the MHRA, with 22 years within the MHRA Inspectorate leading onto several high profile and complex inspections. Tony has been involved in the development of most UK GDP policies and has a deep understanding on the practical application of GDP, the medicines supply chain and the Human Medicines Regulations.
Frequently asked questions

If you have any questions about this course we have answered some of the most common ones below. If you still aren't finding what you're looking for you can contact our team here.

Yes, the RP and GDP course can be delivered in-house for your organisation. This can be arranged as an on-site course at your premises, or as a virtual tutor-led in-house course. Please see our In-house Training page for details. 
Places will be available for you to book unless it states ‘Full’ next to your chosen RP and GDP course date. When this occurs, we operate a waiting list service. 
Yes, we welcome bookings from self-sponsoring individuals. Once your booking has come through to us, we will ask you to complete a new customer form and provide a scanned copy of your photographic ID so that we can raise an account for you on our systems. 
You will need to first register yourself on our booking system by selecting the RP and GDP course date that you wish to book your colleagues onto, then:

 - Add the number of people you wish to book onto the course
 - Register yourself as the booker and complete the fields accordingly
 - Add the details of those you wish to book for
 - Complete your order. 
You will receive an automated email confirming your booking details for the RP and GDP course. 10 days before the start date, if the course is confirmed to run, you will receive another email including the final course details. If the course is to be held virtually, the online registration and joining instructions will also be included.

 

Yes, companies wishing to book multiple employees on one of our standard training courses (excluding IRCA Lead Auditor courses) can benefit from our group booking discount. This discount is only applicable to bookings made for the same course on the same date. Please contact trainingsales@rssl.com with your requirements and we will be happy to provide more information on the best deal available for you. 
Yes, we offer NHS Trusts a 20% discount on ALL our courses, including our Qualified Person training programme. When booking your course/s enter 'NHS' in the discount code field so that your discount can be applied on your invoice. Please note that the NHS discount code is only valid when the booker uses a NHS email address. 
Our online RP and GDP course begins at 09:00am, although we request that you login at 08:30am to ensure any technical glitches can be resolved before the start time. Please review your course confirmation email to double check the exact start time of your specific course.

For our in-person courses, refreshments are available from 08.30am, for a 09:00am start. The standard finish time is 17:00pm, though some courses will finish slightly earlier or later. If you need an exact finishing time to allow for travel arrangements, please contact us via trainingsales@rssl.com or +44 (0)118 918 4000.

As RSSL run all of our virtual courses on Adobe Connect, we recommend that you download the latest version of the Adobe Connect Application at the time of your course - click here to visit the download webpage.


Please see our '
minimum requirements' document for further details on what you'll need to attend our virtual courses. You can test that the Adobe Connect application works for your organisation by completing the RSSL Adobe Connect Function Test. 

Yes, we are more than happy to welcome delegates from all over the world. Our virtual tutor-led courses are particularly popular with international attendees.

All we request is that you have a good understanding of written and spoken English so that you can get the most out of the course. If you wish to attend an in-person course, please also check any visa requirements and await RSSL's full course confirmation before booking your travel to the UK.
Our classroom courses are fully catered, and we provide all refreshments. If you have any special dietary requirements, please enter these into the ‘dietary requirements’ field when creating your account. Our virtual tutor-led courses will include a 45-minute lunch break. 
It is very helpful to have some background knowledge of good distribution practice (GDP) before attending our Responsible Person and GDP Cogent approved course, as there is a knowledge test at the end of the course. So whilst the GDP course is not a prerequisite to being able to attend the RP course, it is certainlu recommended, depending on the level of knowledge you currently have.

There are two GDP course options, our 1 Day Virtual tutor-led GDP course or our eLearning GDP course. Either option will provide a good level of understanding of GDP.
What our clients say

Discover the feedback from our course alumni and learn why they chose RSSL to support their professional development. 

Detailed, interactive and thorough

The course was detailed, interactive, and covered all relevant sections thoroughly. Tutors were very engaging and responsive.
Brian Mzila
The Simple Pharma Company - Quality Manager

Very engaging with great tutors

An engaging course with a great mix of academic knowledge and breakout sessions. The tutors provided valuable industry insights and practical examples.
George Carter
LEXON (UK) LTD - Responsible Person/QA Manager

Covers complex topics well

The course effectively broke down complex topics with group exercises that reinforced learning. Tutors were highly knowledgeable.
Sam Mowbray
AstraZeneca - Quality Facilitator

Well structured and delivered at a good pace

The approach of two trainers kept the course interesting and there was a good mix of work from the screen and breakout sessions. Well structured and delivered at a good pace. Due to the varied nature/background of the attendees I think the course covered the chapters in good detail to enable everyone to understand.
Anonymous
Clinical testing laboratory - Supply Chain and Project Coordinator

Very knowledgeable with plenty of real life examples

Very knowledgeable with plenty of real life examples. Many aspects of the course were interesting and useful for me and I felt a sense of achievement in completing it.
Shaun Sidley
Puro Ventures Ltd t/a Speedy Freight - HSQE Manager

Book Your Place

Responsible Person and GDP Cogent Approved
10 Feb 2025
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Online
22 Apr 2025
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Reading (RSSL)
18 Jun 2025
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Online
08 Sep 2025
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Online
15 Oct 2025
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Reading (RSSL)
01 Dec 2025
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Online
£ excl VAT
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Bespoke Training

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Special Offers

We offer a number of discounts and specials offers on our training courses including Group booking, NHS and Seasonal discounts.

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As scientists ourselves, we’re passionate about collaboration and sharing our expertise to nurture the next generation. By helping them to develop and fulfil their potential, we can tackle 21st-century pharmaceutical scientific challenges more effectively.

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    More than 30 years of experience upskilling pharmaceutical professionals

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    Small-group training adjusted to individual learning styles and needs

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    50+ training courses accredited by recognised industry bodies

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    Combination of off-the-shelf and bespoke training packages

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    Courses and consulting led by experts in the entire pharmaceutical life cycle

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    Opportunity to share and learn as part of a diverse community