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OUR APPROACH: Regulator-e Associates Ltd brings
together the skills of independent regulatory affairs
advisors with many years of scientific experience
in the pharmaceutical industry.
Clients can either contract the services of
individuals, on-site, from our offices, or select
a consultancy package combining the skills of two or
more consultants, you will be guaranteed independent
advice and services.
Our aim is to assist a wide-range of pharmaceutical
companies who are seeking regulatory affairs support.
We currently work with large multinational companies and
smaller companies wishing to expand their portfolio in
Europe. Through our consultants we can assist in
evaluating how current guidelines and legislation can
be used to deliver benefit to the business, and
ultimately set to formalise precise requirements and
specifications for our clients needs. |
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New
Medicines Legislation |
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EU
Clinical Trials Directive |
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Good Clinical Practice |
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Common Technical Document |
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The
Blue Guide |
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Regulator-e House
3 Burton Gardens
Hounslow
Middlesex,
TW5 0DF, United Kingdom
Tel/Fax: +44
(0) 208 572 7875
Mobile: +44 (0) 778 917 3743
E-Mail Address:
info@regulator-e.com
consultants@regulator-e.com |
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