Regulatory Resources Group (RRG) – 20 years on

RRG was established in June 1990 and they have recently celebrated 20 years of successful business.
 
Aug. 18, 2010 - PRLog -- RRG was established in June 1990 and they have recently celebrated 20 years of successful business.

During the past 20 years RRG has offered practical regulatory solutions, often in response to complex and challenging regulatory situations. It is because of the breadth of their regulatory experience that RRG can offer intelligent solutions quickly, saving their client’s time and resource.

As an overview of the breadth of their experience, in brief, over the past 20 years, they have (approx):

• worked on 570 different products  and over 4000 regulatory projects
• submitted Clinical Trial Applications/Marketing Authorisation Applications in 30 European Countries as well as in both the US and Asia
• accumulated over 200 years regulatory experience, in our core internal team of 10 people
• attended over 100 meetings with the Health Authorities on behalf of our clients
• trained over 1000 professionals in regulatory affairs and have helped to foster internal relationships between different disciplines in global and medium sized pharmaceutical companies at many different sites around the world.

RRG attribute their success to their:

• Continuity of service, they always allocate a dedicated project manager for the entire duration of each of their projects, from inception to conclusion.
• Knowledge, each professional that works with them has a minimum of ten years regulatory experience.
• Longevity, having worked in the area for two decades, they have covered all major therapy areas and product formulations.
• Pan European/US expertise. RRG are one of the only regulatory consultancies that has worked with every national regulatory agency in Europe.
• Track record of successful submissions, in accordance with their client’s schedule.
• Ability to coach their clients thought virtual development projects.
• Focus on quality - over 75% of their work is repeat business and over 90% of their business comes from referrals.

Tayce Connolly, Director of RRG, says that ‘it is about continuity, commitment, collaboration and the very high quality of service that we guarantee each of our clients that has sustained us and allowed us to grow the business over the past 20 years. We would like to take this opportunity to thank all of our loyal clients through the years for their commitment to us’.

RRG have established their reputation for adding value and producing quality work in the following areas:

Product Development
Regulatory Strategy and Consultancy
Regulatory Submissions
Training
In-house placements

If you would like any additional information, RRG can be contacted at:

Regulatory Resources Group Ltd.
Innovation House,
Albany Park,
Camberley,
Surrey, GU16 7LP,
England.
Tel: + 44 1276 671166
Fax: +44 1276 670960
Email: mail@rrgconsultancy.com
Website: www.rrgconsultancy.com

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RRG has many years of practical US/EU regulatory experience. RRG provide pharma/biotech clients with global regulatory strategy, product development and regulatory submission support plus comprehensive, bespoke regulatory training programmes.
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Email:***@rrgconsultancy.com Email Verified
Zip:GU16 7PL
Industry:Pharmaceuticals, Consultants
Location:CAMBERLEY - Surrey - England
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