The comprehensive solution for adhering to today’s FDA compliance regulations.
Adhering to FDA cGMP, GLP, and GCP regulations is a complex and daily concern for biotech, pharmaceutical, medical device companies, whether virtual, operating companies, or contract manufacturers. Complya Consulting Group leverages our combined experience in all of these areas to help our clients streamline Quality Assurance and Regulatory Affairs processes and develop standard operating procedures..
We help you maintain FDA-compliant facilities and produce safe and effective products. Our consultants include former VPs and Directors of Quality Assurance and Regulatory Affairs─knowledgeable senior level advisors ready to roll up their sleeves and help you achieve regulatory compliance.
We’re available to work with clients on a short-or long-term basis to manage your Quality Assurance and Regulatory Affairs responsibilities.
Contact us at 617-475-3470 to learn more
Job Opportunities
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Complya is always seeking to expand our team of highly-motivated and skilled GXP Quality Assurance and Regulatory Affairs consultants. Please click on the link below to contact us about our current opportunities.
News & Events
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January 1, 2013 Complya moves to Woburn!
After 5+ years in Cambridge, we've outgrown our office and moved a few miles north to Woburn. Please stop by for a cup of espresso anytime!
December 1, 2012: Complya is moving!
Our new address is: One Presidential Way, Suite 109, Woburn, MA 01801We are excited to announce our upcoming office relocation to Woburn, MA. Although we'll miss being in Cambridge, the new office will allow more space to provide even better service to both our customers and to our consulting partners. More details coming soon!
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