SEQ Regulatory Affairs Consultants is a privately owned company, with a well established reputation and experience in the pharmaceutical industry in Pharmaceutical Licensing and Business Development and as a provider of Regulatory Services from regulatory strategy to approval grant.
SEQ adds value to its clients by increasing efficiency, reliability and profitability in maximising product development. SEQ have project managed products including POM, OTC, CE marking & Herbal medicinal, in the full range of dosage forms through National or European submission routes, using the advanced submission Management System for eCTD and lifecycle management. Our services can be tailored to meet your specific needs.
SEQ have been in the pharmaceutical industry for over 30 years, helping 100’s of companies achieve success.
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