Complya Consulting Group

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

Join Us

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

  • On the Road with Complya

    Please join us at these upcoming events!

    September 15, 2011: New England Parenteral Drug Association

    Complya is pleased to sponsor the "Analytical Method Development and Validation" meeting with Stephan O. Krause, Ph.D (MedImmune) and Clifton E. McPherson, Ph.D (Protein Sciences Corp.) scheduled as speakers.

    September 19-21, 2011: PDA/FDA Joint Regulatory Conference

    Complya will be exhibiting at this annual meeting with the FDA in Washington, DC. Please stop by our booth to say hello!

    For more information, please visit their website.

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