Global Regulatory Services

Bobby Deal is a visionary who embraces new technologies and new markets.  Throughout his extensive career he has remained passionate about medicine and healthcare not only for human health but also animal health.  His enthusiasm is infectious! 

He is hard working, quick thinking, adaptable and has lots of patience with a good sense of humour and a passion for life and believes it is essential to laugh every day.  Everyone who works with him will have fun along the way.  He has a great sense of humour, getting on well with people from all walks of life and looks forward to facing new challenges every day.

Specifically, his role is business growth and development with the aim of nurturing long-term relationships with all GRS clients offering them robust and, where necessary and appropriate, innovative solutions for the development of their medical products.  If you have a question but you’re not sure who to ask then, please, do not hesitate to have a chat with Bobby because he will be able to find the answer amongst the GRS network of professionals and Subject Matter Experts.

Owner-Managing Director

Med-Di-Dia Limited

Med-Di-Dia, a subsidiary of Global Regulatory Services, is a consultancy focusing on regulatory affairs and quality compliance for the European Medical, Digital Health and Diagnostics sectors.  With passion and drive we have the flexibility to provide a cost-effective, bespoke solution which exactly fits the needs of you, the client.

With the significant changes taking place due to updated regulations and the changing political scene, we can provide stability and expertise to UK and non-EU based organisations in need of an EU presence at an affordable price.  

Specific services include:

	Person Responsible
For micro and small companies, we will be your Person Responsible under the new EU Medical Device and In-Vitro Diagnostic Regulations.

	Authorised Representative
For non-EU and UK companies, we can be your Authorised Representative within Europe.

	Legal Representative for EU Clinical Trials
For UK organisations running EU-wide clinical trials, we will be happy to act as your Legal Representative to ensure continuity of your trials post-Brexit at a minimal cost.

Ongoing and routine services:
	Help to define your product and develop your regulatory strategy
	Expertise to ensure a successful EU CE Mark registration
	Technical File and Design File compiliations
	Design control (verification and validation)
	Software validation
	Risk Management Analysis
	Clinical Evaluations and Clinical Investigation Plans
	Quality Management Systems (QMS)
	Submissions and registration management
	Liaising with Competent Authorities and Notified Bodies
	Notified Body Selection

Crème de la Crème Limited

Crème de la Crème is dedicated to providing regulatory advice and support exclusively to the Cosmetic Industry with a particular focus on the requirements of the European Cosmetic Products Regulation (EU Regulation 1223/2009).  Recognising that every company is unique, we will provide a bespoke service so that you have the support and guidance which exactly fits your needs.  Our services range from conducting a label review to being your Responsible Person.

Hard working, quick thinking with a passion for life.  

I love connecting with people on LinkedIn so that we can exchange ideas, share knowledge and develop a professional relationship for the long-term.  It's also great to reach out to my LinkedIn connections if ever I should need help or advice.  Please, oh please, if I do accept your invitation to connect, do not sell me anything and especially not in our first message exchange. Thank you!


Taplio

Bobby Deal's Linkedin Analytics

Want to drive more opportunities from LinkedIn?

Taplio

.css-1jgreyo{background-image:linear-gradient(284deg, rgba(39,43,72,1) 0%, rgba(33,47,183,1) 100%);color:transparent;-webkit-background-clip:text;background-clip:text;}Bobby Deal's Linkedin Analytics

Want to drive more opportunities from LinkedIn?

Bobby Deal's Linkedin Analytics