Regulatory Affairs Consultants
& Medical Writing Services
Since 2005, we've built our reputation for fast, reliable and responsive EU regulatory affairs consulting with major healthcare companies worldwide.
We provide regulatory consulting and medical writing solutions for you at every stage of your pharmaceutical product's lifecycle. We can deliver high level regulatory strategy, meet unexpected resource demands and provide cost-effective regulatory submissions.
Download our brochure now, or request a brochure by post.
We can help you with:
We provide strategic and flexible regulatory affairs consulting services across all phases of development. Find out more.
We can manage all your regulatory submissions requirements, both for new chemical entities and for maintenance work in all submission formats including eCTD. Find out more.
We deliver extensive expertise in medical writing across numerous document types and therapeutic areas. Find out more.
From Risk Management Plans to Periodic Safety Update Reports (PSURs), we ensure you meet your pharmacovigilance commitments. Find out more.
Having conducted over 700 Patient Information Leaflet Tests we're acknowledged experts in the field of readability testing. Find out more.
We can help you with all aspects of your Health Technology Appraisal (HTA), consultancy, submission development, medical writing & economic analyses.
Find out more.
Call us today to talk about your project on +44 (0)1403 320280.
Download our brochure now, or request a brochure by post.
©2011 Spectrum Regulatory Solutions
Spectrum Regulatory Solutions, Fraser House, 14 Carfax, Horsham, West Sussex RH12 1DZ regulate@spectrumrs.com. Spectrumrs.com is the trading name of Spectrum Regulatory Solutions Ltd. Spectrum Regulatory Solutions is a limited company registered in England and Wales with company number 5331222. Registered office: St James's House, 8 Overcliffe, Gravesend, Kent DA11 0HJ. VAT registration no: 818283318
