The comprehensive solution for adhering to today’s FDA regulations. Complying to FDA cGMP, GLP, and GCP regulations is a complex and daily concern for biotechnology, pharmaceutical and medical device companies, whether virtual organizations, operating companies, or contract manufacturers. Complya Consulting Group leverages our combined experience in all of these areas to help our clients increase compliance, accelerate timelines, and shorten their to-do lists.
Complya News & Events
- 04.14.2016 || Join Complya at the next NEPDA Meeting on May 18, 2016
- 04.13.2016 || Complya Consulting & MPI Release Joint Whitepaper on Aseptic Processing
- 03.22.2016 || Join Complya at the SQA Annual Meeting & Quality College
- 02.01.2016 || Join Complya at the NSTC First Friday Bioscience!