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
- 02.26.2015 || Complya Virtual Toolbox Case Study
- 02.05.2015 || Complya President Elected NE PDA President
- 01.21.2015 || Join Complya at the next NE PDA Meeting on March 11, 2015
- 01.15.2015 || Join Complya at the SQA Annual Meeting & Quality College April 12-17, 2015