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
- 05.05.2015 || Join Complya at the next NE PDA Meeting on May 13, 2015
- 04.07.2015 || Join Complya at ASQ BOSCON on April 14, 2015
- 02.26.2015 || Complya Virtual Toolbox Case Study
- 02.05.2015 || Complya President Elected NE PDA President