Our closest colleagues serving the life sciences community.
These trusted colleagues share our values and have met our highest standards of service and expertise.
CRS is a US-owned and operated contract research organization and executive management consultancy for start-up and mid-size life sciences companies with a mission to improve their performance and provide a successful clinical research development plan and strategy. CRS works with life science start-ups, medical device companies and large pharma.
Michelle Lott helps clients recognize regulatory and quality issues aren’t a “burden” – they are strategic advantages when used properly. Her expert team will also strip away any redundant or misdirected activities so you can focus on what really matters: Winning in the marketplace!
The Evanston Group is a life sciences consulting firm providing specialty talent to the industry’s largest global leaders. With 4,000 engagements since our founding in 1999, we find amazing people to help do amazing things when you need high-caliber expertise.
Levine Tox Consulting provides consultation services in all phases of nonclinical drug development and in product liability/forensic toxicology issues. Experience includes several classes of small molecules, biologics including proteins and monoclonal antibodies, and biosimilars.
Aquila Solutions will convert your regulatory application/submission into an electronic Common Technical Document (eCTD) format, which is the format required by the FDA. Aquila will provide minor editorial revision and formatting, if required. Aquila also can help with your Structured Product Label Authoring (SPL) needs. On completion, you can submit your electronically formatted application to the FDA or Aquila can do this for you.