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
- 02.20.2017 || SQA 2017 Exhibitor
- 02.14.2017 || 2017: Significant Changes for the Pharmaceutical Industry
- 10.27.2016 || Insights into the 2017 U.S. Regulatory Landscape
- || Key EU Deadlines for Q4 2016 and Early 2017